co_sos
1 records
CO Business: ABBOTT LABORATORIES INC.
2003-08-15
FPC | Status: Good Standing | Abbott Park, IL
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CourtListener
1 records
Court Opinion: Abbott Laboratories v. H&H Wholesale Services, Inc.
2016-11-03
Court of Appeals for the Second Circuit | Docket: No. 15-3785-cv(L), No. 15-3858-cv(CON) | Cited 9x
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courtlistener_docket
13 records
Mahan v. Abbott Laboratories, Inc.
2026-06-03
Federal docket 1:26-cv-06561 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Frost v. Abbott Laboratories, Inc.
2026-06-02
Federal docket 0:26-cv-02820 (mnd); matched party 'Abbott Laboratories, Inc.'
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O'Malley v. Abbott Laboratories, Inc.
2026-06-02
Federal docket 1:26-cv-06411 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Warren v. Abbott Laboratories, Inc.
2026-06-01
Federal docket 8:26-cv-00247 (ned); matched party 'Abbott Laboratories, Inc.'
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Ghosh v. Abbott Laboratories, Inc.
2026-05-29
Federal docket 1:26-cv-00264 (hid); matched party 'Abbott Laboratories, Inc.'
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O'Malley v. Abbott Laboratories, Inc.
2026-05-14
Federal docket 1:26-cv-00482 (ohsd); matched party 'Abbott Laboratories, Inc.'
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Catron v. Abbott Laboratories, Inc.
2026-05-13
Federal docket 1:26-cv-05572 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Henderson v. Abbott Laboratories, Inc.
2026-05-06
Federal docket 1:26-cv-05270 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Gandy v. ABBOTT LABORATORIES, INC. D/B/A ABBOTT NUTRITION
2026-04-13
Federal docket 1:26-cv-04119 (ilnd); matched party 'ABBOTT LABORATORIES, INC. D/B/A ABBOTT NUTRITION'
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Mulhall v. Abbott Laboratories, Inc.
2026-04-02
Federal docket 1:26-cv-03691 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Braden v. Abbott Laboratories, Inc.
2026-03-31
Federal docket 1:26-cv-03562 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Moctezuma v. Abbott Laboratories, Inc.
2026-03-27
Federal docket 1:26-cv-03404 (ilnd); matched party 'Abbott Laboratories, Inc.'
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Johansen v. Abbott Laboratories, Inc.
2026-03-26
Federal docket 1:26-cv-03322 (ilnd); matched party 'Abbott Laboratories, Inc.'
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EPA (Environmental Protection Agency)
3 records
epa_echo
9 records
EPA ECHO: ABBOTT LABORATORIES
1997-10-02
Penalty assessed: $7,200. Type: Administrative - Formal
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EPA ECHO: ABBOTT LABORATORIES
1997-08-13
Penalty assessed: $182,654. Type: Administrative - Formal
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EPA ECHO: ABBOTT LABORATORIES, INC.
1994-12-19
Penalty assessed: $28,000. Type: Administrative - Formal
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EPA ECHO: ABBOTT LABORATORIES, INC.
1994-10-31
Penalty assessed: $28,000. Type: Administrative - Formal
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fda
146 records
FDA Recall: Abbott Laboratories — Class II
20250430
When expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user tha | Product: Brand Name: CELL-DYN Ruby Product Nam...
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FDA Device Recall: Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20
2025-12-24
Class II — Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues fou...
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FDA Device Recall: Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalo
2025-11-19
Class II — Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results.
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FDA Device Recall: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08
2025-04-30
Class II — When expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use...
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FDA Device Recall: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08
2025-04-30
Class II — When expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use...
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FDA Device Recall: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08
2025-04-30
Class II — When expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use...
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FDA Recall: Abbott Laboratories — Class II
20240103
There are potential performance issues found in the Alinity ci-series System software versions 3.4.0 and lower, including: 1) SCC Reagent load error d | Product: Alinity ci-series System Control Modul...
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FDA Device Recall: Alinity hq Analyzer, REF: 09P68-01
2024-08-28
Class II — 1)If Complete Blood Count with differential and reticulocyte(CBC+Diff+Retic) sample is run, then immediately following on same rack CBC+Diff sample is run, then falsely low red blood cell c...
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FDA Device Recall: ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.
2024-04-10
Class II — The reason for the recall is the failure of calibration and quality controls due to a manufacturing issue of microparticles not meeting labeled claim. This may lead to incorrect myoglobin ...
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FDA Device Recall: Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is
2024-01-17
Class II — The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).
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FDA Device Recall: Alinity c Processing Module REF 03R67-01 The Alinity c Processing Module is
2024-01-17
Class II — The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).
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FDA Device Recall: ARCHITECT c4000 Processing Module REF: 02P24-01 02P24-02 02P24-40 01R24-56
2024-01-17
Class II — The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).
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FDA Device Recall: Alinity ci-series System Control Module, REF: 03R70-01
2024-01-03
Class II — There are potential performance issues found in the Alinity ci-series System software versions 3.4.0 and lower, including: 1) SCC Reagent load error during daily maintenance; 2) Sample Labo...
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FDA Recall: Abbott Laboratories — Class II
20230419
Potential of foreign material (hard plastic) within product | Product: Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per ca
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FDA Device Recall: Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN S
2023-12-27
Class II — The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).
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FDA Food Recall: Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil
2023-11-15
Class II — Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive
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FDA Food Recall: Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individ
2023-04-19
Class II — Potential of foreign material (hard plastic) within product
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FDA Device Recall: Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITEC
2023-01-25
Class III — Reaction vessels may contain a potential contaminant that could affect their optical performance.
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FDA Recall: Abbott Laboratories — Class II
20221123
Compromised seal integrity which could lead to spoilage | Product: Similac 360 Total Care 2 fl oz reclose able plastic bottle Packaged as: 6 count carton, 12 count ca
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FDA Recall: Abbott Laboratories — Class II
20221123
Compromised seal integrity which could lead to spoilage | Product: Similac Neosure 2 fl oz reclose able plastic bottle Packaged as: 48 count case
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FDA Recall: Abbott Laboratories — Class II
20221123
Compromised seal integrity which could lead to spoilage | Product: Similac 360 Total Care Sensitive 2 fl oz reclose able plastic bottle Packaged as: 6 count carton, 1
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FDA Recall: Abbott Laboratories — Class II
20221123
Compromised seal integrity which could lead to spoilage | Product: Similac 360 Total Care/Similac 360 Total Care Sensitive Discharge Kit 2 fl oz reclose able plastic
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FDA Recall: Abbott Laboratories — Class II
20220803
There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c | Product: REF: 08P4377, Alinity c Hemoglobin R...
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FDA Recall: Abbott Laboratories — Class II
20220629
These products are being recalled due to the potential of leakage from the 1L container. | Product: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor
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FDA Recall: Abbott Laboratories — Class III
20220622
The third party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder, which is not declare | Product: Pedialyte***Replaces Electrolytes***Gr...
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FDA Recall: Abbott Laboratories — Class I
20220316
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil | Product: Abbott Similac Advance Infant Formula ...
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FDA Recall: Abbott Laboratories — Class I
20220316
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil | Product: Abbott Alimentum, Abbott Similac Alime...
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FDA Recall: Abbott Laboratories — Class I
20220316
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil | Product: Abbott Similac for Supplementation 22o...
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FDA Recall: Abbott Laboratories — Class I
20220316
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil | Product: Abbott Similac Pro-Advance 23oz. and 3...
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FDA Recall: Abbott Laboratories — Class I
20220316
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil | Product: Abbott Similac For Spit Up Infant Form...
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FDA Recall: Abbott Laboratories — Class I
20220316
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facil | Product: Abbott Similac Human Milk Fortifier 0....
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FDA Food Recall: Similac 360 Total Care 2 fl oz reclose able plastic bottle Packaged as: 6 count
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac Neosure 2 fl oz reclose able plastic bottle Packaged as: 48 count case
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac 360 Total Care Sensitive 2 fl oz reclose able plastic bottle Packaged a
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac 360 Total Care/Similac 360 Total Care Sensitive Discharge Kit 2 fl oz r
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac Total Comfort 2 fl oz reclose able plastic bottle Packaged as: 12 - 4 p
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac 360 Total Care Sensitive with Nipples 2 fl oz reclose able plastic bottl
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac Water - Sterilized (Export Canada) 2 fl oz reclose able plastic bottle
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac Special Care 2 fl oz reclose able plastic bottle Packaged as: 4 count c
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Similac Stage 1 (Export Dominican Republic) 2 fl oz reclose able plastic bottle
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Food Recall: Pedialyte Unflavored (Export to Canada) 2 fl oz plastic reclosable bottle 48 cou
2022-11-23
Class II — Compromised seal integrity which could lead to spoilage
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FDA Device Recall: ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
2022-09-07
Class II — One lot of reagent was manufactured with insufficient quantities of the heterophilic blocking agents in the conjugate component.
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FDA Food Recall: Abbott Jevity Complete, Balanced Nutrition with Fiber Ready to Hang enteral feed
2022-08-31
Class II — Potential leaking/pinholes in bottle
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FDA Device Recall: REF: 08P4377, Alinity c Hemoglobin Reagent Kit, IVD, CE, R1 5 x 46.0 mL, R2 5
2022-08-03
Class II — There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
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FDA Device Recall: REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1
2022-08-03
Class II — There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
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FDA Device Recall: REF: 08P4320, Alinity c Hemoglobin Reagent Kit, IVD, CE, R1 5 x 46.0 mL, R2 5
2022-08-03
Class II — There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
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FDA Food Recall: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural
2022-06-29
Class II — These products are being recalled due to the potential of leakage from the 1L container.
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FDA Food Recall: Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry Lemon
2022-06-22
Class III — The third party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder, which is not declared on the label.
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FDA Device Recall: Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)003807401
2022-03-23
Class II — Software error associated with the immunoassay analyzer wash cycle which is using 1 mL of wash buffer instead of the intended 3 mL of wash buffer to wash the exterior of the probe.
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FDA Food Recall: Abbott Similac Advance Infant Formula with Iron 12.4oz. can, 23.2oz. plastic jar
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Alimentum, Abbott Similac Alimentum, Abbott Similac Alimentum HMO, Abbott
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac for Supplementation 22oz. plastic jar. 4 jars per case. Item
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Pro-Advance 23oz. and 34oz. plastic jar. 6 jars per case. Ite
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac For Spit Up Infant Formula with Iron 22.5oz plastic jar. 6 jars
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Human Milk Fortifier 0.9g Pouch / Sachet, 50 Pouch / Sachet per r
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac For Spit Up Infant Formula with Iron 7oz. can and 19.5oz. plastic
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Organic 7oz. can. 6 cans per case. Abbott Similac Organic with A
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Sensitive Infant Formula with Iron 22.5oz. plastic jar. 6 jars p
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Sensitive 34oz. plastic jar. 6 jars per case. Abbott Similac Se
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Alimentum Eye Q Plus 400g. can. Abbott Alimentum Eye Q 400g. can.
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Advance Step-2 22.5oz. plastic jar. 6 jars per case. Abbott Sim
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Pro-Advance 20.6oz., 30.3oz., 34oz., and 658g plastic jar. 6 jars
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac 360 Total Care Sensitive Infant Formula with Iron 7oz. can. 6 can
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Alimentum Allergies & Colic Hypoallergenic Infant Formula 400g. c
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Advance Step-1 22oz. plastic jar and 34 oz. can. 6 units per cas
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Organic with A2 Milk Toddler Drink 23.2oz plastic jar. 4 jars per
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Total Comfort 638g. plastic jar and 8oz. can. 6 units per case.
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Total Comfort 12.6oz. can. 6 cans per case. Item numbers: 62
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Alimentum 400g. can. 6 cans per case. Item numbers: 5705806
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Total Comfort Infant Formula with Iron 12.6oz. can. 6 cans per ca
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare Jr Amino Acid-Based Nutrition Powder Chocolate 14.1oz. can. 6 ca
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac 360 Total Care Infant Formula with Iron 20.6oz. and 30.3oz. palst
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare Jr Amino Acid-Based Nutrition Powder Banana 14.1oz. can. 6 cans
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac For Spit Up Infant Formula with Iron 12.5oz. can. 6 cans per case
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare Infant Formula Unflavoured 400g can. 6 cans per case. Item numb
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Pro-Total Comfort Infant Formula with Iron 20.1oz. and 22.5oz. pl
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Alimentum with 2'-FL HMO, Abbott Similac Alimentum HMO, Abbott Al
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare Amino Acid-Based Powder Infant Formula with Iron 14.1oz. can, Abb
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare Junior Vanilla 14.1oz. can and Abbott EleCare Jr Similac Vanilla
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g. can. 6 cans pe
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott Similac Sensitive Lactose Sensitivity 22oz. plastic jar. 6 jars per case
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Food Recall: Abbott EleCare Jr Amino Acid-Based Nutrition Powder Unflavored 14.1oz. can. 6 c
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
View Source
FDA Food Recall: Abbott Similac Alimentum Toddler Drink 12.1oz. can. 6 cans per case. Item nu
2022-03-16
Class I — Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
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FDA Recall: Abbott Laboratories, Inc — Class II
20210818
A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators. | Product: Alinity s System REF 06P16-01. An automated immunoassay analyzer fo...
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FDA Recall: Abbott Laboratories — Class II
20210811
There is a potential for >10% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than 1,200 U/L. In addition there is a pote | Product: REF 8L92-42, Abbott Activated Alanine ...
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FDA Device Recall: ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M7
2021-12-01
Class II — Twelve software-related issues affecting software version 9.41 and earlier were identified. The issues include bypassing error codes, incorrect calibration, loss of module communication lea...
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FDA Device Recall: Alinity ci-series System Control Module clinical chemistry and immunoassay analy
2021-09-22
Class II — Due to potential performance issues with software version 3.2.3 and earlier. Performance issues are: 1) There is the potential for onboard reagents past their lot expiration date or onboa...
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FDA Device Recall: Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro
2021-08-18
Class II — A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators.
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FDA Device Recall: REF 8L92-42, Abbott Activated Alanine Aminotransferase, for use with Architect,
2021-08-11
Class II — There is a potential for >10% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than 1,200 U/L. In addition there is a potential for a >10% shift in patient resul...
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FDA Device Recall: REF: 08P1820, Abbott Alinity c Activated Alanine Aminotransferase reagent Kit,
2021-08-11
Class II — There is a potential for 15% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than 1,200 U/L. In addition there is a potential for a >10% shift in patient result...
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FDA Recall: Abbott Laboratories, Inc — Class II
20200415
Mixer blade may separate from mixer due to the screw and nut failure and detachment. As a result of the mixer blade missing, the sample and reagent ar | Product: ARCHITECT C System Mixer - Product Usa...
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FDA Device Recall: ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis
2020-05-13
Class III — Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.
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FDA Device Recall: ARCHITECT C Peptide Reagent - Product Usage: used as an aid in the diagnosis and
2020-05-13
Class III — Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.
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FDA Device Recall: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry Syste
2020-04-15
Class II — Mixer blade may separate from mixer due to the screw and nut failure and detachment. As a result of the mixer blade missing, the sample and reagent are inadequately mixed.
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FDA Recall: Abbott Laboratories, Inc — Class II
20190731
An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with | Product: C4 is an in vitro diagnostic assay for...
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FDA Recall: Abbott Laboratories — Class III
20190522
Devices were delivered without the required dry ice. | Product: ARCHITECT Intact PTH Calibrators - Product Usage: The ARCHITECT Intact PTH Calibrators are for the c
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FDA Recall: Abbott Laboratories — Class III
20190522
Devices were delivered without the required dry ice. | Product: ARCHITECT STAT High Sensitive Troponin-I Calibrators - Product Usage: The ARCHITECT STAT High Sensi
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FDA Recall: Abbott Laboratories — Class III
20190522
Devices were delivered without the required dry ice. | Product: ALINITY i Anti-TPO Calibrators - Product Usage: The Alinity i Anti-TPO Calibrators are for the calib
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FDA Recall: Abbott Laboratories — Class II
20190410
There is a potential for the device to generate Quality Control (QC) low or out-of-range low for parameters RBC and PLT. | Product: CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is...
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FDA Device Recall: Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald inst
2019-10-30
Class II — The diluent tubing used on the instrument appears cloudy or to have a powder/film on the inner and outer surfaces which may result in falsely elevated platelet results.
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FDA Food Recall: Abbott Calcilo XD, Low-calcium Vitamin D-Free Infant formula with iron, powder i
2019-10-16
Class II — Off color and odor. Compromised can seam due to product (powder) in the seam, this poor seal potentially allowed air into the container.
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FDA Device Recall: APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2
2019-10-02
Class II — The firm identified customer sites where modules which the safety pacemaker label is missing. Information regarding the label included in the Operations Manual has been updated to specify: ...
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FDA Device Recall: C4 is an in vitro diagnostic assay for the quantitative determination of C4 in h
2019-07-31
Class II — An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
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FDA Device Recall: ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are f
2019-07-31
Class III — Presence of a time dependent, stability drift in patient and control results returned from ARCHITECT BNP testing.
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FDA Device Recall: ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are for th
2019-07-31
Class III — Presence of a time dependent, stability drift in patient and control results returned from ARCHITECT BNP testing.
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FDA Device Recall: Immunoglobulin M is an in vitro diagnostic assay for the quantitative determinat
2019-07-31
Class II — An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
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FDA Device Recall: Apolipoprotein A1 is an in vitro diagnostic assay for the quantitative determina
2019-07-31
Class II — An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
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FDA Device Recall: Immunoglobulin A is an in vitro diagnostic assay for the quantitative determinat
2019-07-31
Class II — An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
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FDA Device Recall: Immunoglobulin G is an in vitro diagnostic assay for the quantitative determinat
2019-07-31
Class II — An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
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FDA Device Recall: Apolipoprotein B is an in vitro diagnostic assay for the quantitative determinat
2019-07-31
Class II — An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
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FDA Device Recall: ARCHITECT Intact PTH Calibrators - Product Usage: The ARCHITECT Intact PTH Calib
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: ARCHITECT STAT High Sensitive Troponin-I Calibrators - Product Usage: The ARCHI
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: ALINITY i Anti-TPO Calibrators - Product Usage: The Alinity i Anti-TPO Calibrato
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: Technopath Multichem S Plus Level 2 - Product Usage: Multichem S Plus (Assayed)
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: ARCHITECT STAT High Sensitive Troponin-I Controls - Product Usage: The ARCHITECT
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: Technopath Multichem S Plus Level 1 - Product Usage: Multichem S Plus (Assayed)
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: ARCHITECT HbA1C Calibrators - Product Usage: The ARCHITECT HbA1c Calibrators are
2019-05-22
Class III — Devices were delivered without the required dry ice.
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FDA Device Recall: Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHI
2019-05-15
Class II — There is a potential to generate falsely elevated serum or plasma chloride results when using the product.
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FDA Device Recall: Abbott ARCHITECT c4000 Processing Module, List No. 02P24 - Product Usage: The Ab
2019-04-17
Class II — There is a potential to generate incorrect results on the instrument if particular error codes are not resolved before transitioning to the Running status.
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FDA Device Recall: Abbott ARCHITECT c16000 Processing Module, List No. 03L77 - Product Usage: The A
2019-04-17
Class II — There is a potential to generate incorrect results on the instrument if particular error codes are not resolved before transitioning to the Running status.
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FDA Device Recall: CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automate
2019-04-10
Class II — There is a potential for the device to generate Quality Control (QC) low or out-of-range low for parameters RBC and PLT.
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FDA Device Recall: Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.
2019-04-10
Class II — The product has a stability issue which may lead to an error code indicating "Unable to calculate result, reaction check failure" and/or Quality Control results out of range low.
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FDA Device Recall: ARCHITECT MAGNESIUM, (a) REF 7D70-21, (b) 7D70-31 The Magnesium assay is used
2019-03-13
Class II — Abbott internal testing has identified that the Magnesium urine application demonstrates depressed urine result recovery. All samples >0.5mEq/L fail the linearity acceptance criteria for th...
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FDA Recall: Abbott Laboratories, Inc. — Class II
20180801
Abbott is advising customers that a small number of CardioMEMS(R) Hospital Electronics Systems (Model CM3000) and Patient Electronics Systems (Model C | Product: CardioMEMS HF System Hospital and Pati...
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FDA Device Recall: CardioMEMS HF System Hospital and Patient Electronics Units: (a) Patient Electr
2018-08-01
Class II — Abbott is advising customers that a small number of CardioMEMS(R) Hospital Electronics Systems (Model CM3000) and Patient Electronics Systems (Model CM1100) may deliver a system error, know...
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FDA Device Recall: ARCHITECT c8000 Cuvette Segment, Part #01G46-01/01G06, a component to the ARCHIT
2018-03-14
Class II — There is a potential to generate falsely depressed patient results in the cuvettes adjacent to the detached segment post for any assay run on the c4000, c8000, and c16000 instrument.
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FDA Device Recall: ARCHITECT c4000 Cuvette Segment, Part #02P75-01/02P24, a component to the ARCHIT
2018-03-14
Class II — There is a potential to generate falsely depressed patient results in the cuvettes adjacent to the detached segment post for any assay run on the c4000, c8000, and c16000 instrument.
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FDA Recall: Abbott Laboratories, Inc — Class II
20171129
The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with | Product: ARCHITECT c4000 part number 02P24; ARC...
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FDA Device Recall: ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT
2017-11-29
Class II — The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.
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FDA Device Recall: ARCHITECT c4000 Cuvette Segment, List number 02P75-01. The firm name on the lab
2017-10-18
Class II — There is a potential to generate falsely-depressed patient results in the cuvettes adjacent to the detached segment post for any assay run on the c4000 instrument.
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FDA Device Recall: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent micropa
2017-06-28
Class II — Firm has identified that ARCHITECT SHBG results generated with the Potassium EDTA specimen tube type may demonstrate a negative shift relative to results generated with serum. There is a p...
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FDA Device Recall: CELL-DYN Ruby System: List Number: 08H6701; Hematology: The CELL-DYN Ruby
2017-03-15
Class II — The Pump Relay Printed Circuit Board Assembly (PCBA) used in the CELL-DYN Ruby instrument may prematurely fail and lead to instrument stoppage
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FDA Recall: Abbott Laboratories — Class II
20160608
Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to falsely elevated estradiol results in patients treated with Fulvestrant. | Product: The ARCHITECT Estradiol Kit Intended t...
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FDA Device Recall: ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay is used for the
2016-11-16
Class II — Abbott has identified negative interference from the drug N-Acetyl Cysteine (NAC) with the ARCHITECT Lactic Acid reagent (LN 9D89-21).
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FDA Device Recall: The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic ste
2016-06-08
Class II — Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to falsely elevated estradiol results in patients treated with Fulvestrant.
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FDA Device Recall: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHIT
2015-07-29
Class II — The ARCHITECT c8000 instrument contains tubing that does not meet specifications and has the potential to leak.
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FDA Food Recall: Similac¿ Advance Complete Nutrition Infant Formula with Iron, 1.45lb plastic con
2015-03-18
Class II — The firm received three consumer calls of product with Chinese labeling. After an internal investigation, the firm discovered that product manufactured for export to China was distributed ...
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FDA Device Recall: HbA1c Calibrators LN 4P52-02 consists of: 4P52-02 Hemoglobin A1c 1 x 1.6 mL and
2014-11-05
Class II — HbA1c Calibrators LN 4P52-02, lot 45063UQ12 may contain a value sheet for a different HbA1c calibrator lot. If calibrator lot 45063UQ12 is used in the calibration of the HbA1c assay using v...
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FDA Recall: Abbott Laboratories, Inc — Class II
20130424
Abbott Diagnostics is recalling Clinical Chemistry Phenobarbital reagent lots 62299UN12 and 85773UN12 due to imprecision issues which increase with th | Product: Clinical Chemistry Phenobarbital, list...
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FDA Device Recall: Clinical Chemistry Phenobarbital, list number 1E08
2013-04-24
Class II — Abbott Diagnostics is recalling Clinical Chemistry Phenobarbital reagent lots 62299UN12 and 85773UN12 due to imprecision issues which increase with the age of the reagent lot. The imprecis...
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FDA Device Recall: Abbott Laboratories, ARCHITECT 25-OH Vitamin D Reagent Kit, 03L52-25 (ROW) and 0
2013-01-30
Class II — The Architect 25-OH Vitamin D assay has the potential to generate falsely elevated or falsely depressed results when used with certain lots of Architect Reaction Vessels.
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FDA Drug Recall: Synthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bott
2013-01-09
Class II — Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
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FDA Drug Recall: Synthroid (levothyroxine sodium) Tablets USP, 112 mcg, Rx Only, 90-Count Bottle,
2012-10-03
Class II — Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
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FDA Drug Recall: Synthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle,
2012-10-03
Class II — Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
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FDA Drug Recall: Synthroid (levothyroxine sodium) Tablets USP, 50 mcg, Rx Only, 90-Count Bottle,
2012-10-03
Class II — Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.
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FDA Drug Recall: Zemplar (paricalcitol) Injection, 5 mcg/mL in 2 mL multi-dose vials, 25 vial car
2012-06-27
Class II — CGMP Deviations: There is potential that Abbott's third party manufacturer, Hospira, may have applied a foreign (incorrect) stopper to vials in a specific lot of Zemplar Injection.
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ftc
2 records
FTC Case: Abbott Laboratories, In the Matter of
FTC enforcement action — tags: enforcement
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FTC Case: Abbott Laboratories, In the Matter of
FTC enforcement action — tags: enforcement
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ftc_enforcement
2 records
Abbott Laboratories, In the Matter of
2000-05-26
FTC live enforcement action FY2000; matched respondent 'Abbott Laboratories, In the Matter of'
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Abbott Laboratories, In the Matter of
1997-06-06
FTC live enforcement action FY1997; matched respondent 'Abbott Laboratories, In the Matter of'
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lobbying
12 records
Lobbying Client: ABBOTT LABORATORIES
Lobbied by TIBER CREEK GROUP — Medical Device and Healthcare Company.
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by S-3 GROUP — Healthcare technology company
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by MARSHALL & POPP, LLC — Health care company with medical devices, diagnostics and nutrition.
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by KOUNTOUPES DENHAM CARR & REID, LLC — Healthcare company with innovative medical devices, diagnostics and nutrition.
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by AKIN GUMP STRAUSS HAUER & FELD — Healthcare
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by MARSHALL & POPP, LLC — Health care company with medical devices, diagnostics and nutrition.
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by S-3 GROUP — Healthcare technology company
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by TIBER CREEK GROUP — Medical Device and Healthcare Company.
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Lobbying Client: ABBOTT LABORATORIES
Lobbied by AKIN GUMP STRAUSS HAUER & FELD — Healthcare
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ny_corps
1 records
NY Corp: ABBOTT LABORATORIES
1901-08-26
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Illinois
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SEC EDGAR
1 records
USASpending
33 records
Federal Award: ABBOTT LABORATORIES INC. — $3,378,771
2026-04-01
EMERGENCY FOR CHEMISTRY CPRR WITH AUTOMATION
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Federal Award: ABBOTT LABORATORIES INC. — $1,198,000
2025-10-01
CHEMICAL ANALYSIS INSTRUMENTS
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Federal Award: ABBOTT LABORATORIES INC. — $1,688,329
2025-01-01
ABBOTT ALINITY CI ANALYZER COST-PER-REPORTABLE
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Federal Award: ABBOTT LABORATORIES INC. — $11,358,292
2024-04-01
VISN 9 CHEMISTRY AUTOMATION COST PER RESULTS REPORTABLE
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Federal Award: ABBOTT LABORATORIES — $65,469,511
2022-09-21
ABBOTT: TO CONDUCT CLINICAL TRAINING AND VALIDATION STUDIES TO SUPPORT A FUTURE FDA MARKETING APPLICATION WITH AN EXPANDED INDICATION FOR USE OF THE ABBOTT TBI TEST ? TO AID IN THE
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Federal Award: ABBOTT LABORATORIES INC. — $2,903,748
2022-03-15
ISTAT POINT OF CARE SYSTEM
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Federal Award: ABBOTT LABORATORIES INC. — $1,558,414
2021-01-01
ISTAT ANALYZERS & CARTRIDGES
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Federal Award: ABBOTT LABORATORIES INC. — $4,602,564
2019-04-25
ABBOTT LABORATORIES:1107303 [19-009467]
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Federal Award: ABBOTT LABORATORIES INC. — $37,604,629
2019-03-01
LABORATORY ASSAY FOR TRAUMATIC BRAIN INJURY
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Federal Contractor: ABBOTT LABORATORIES INC.
Total awards: $116,430,719 | UEI: L3AXXYLB3V56 | DUNS: 967474896
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Federal Contractor: ABBOTT LABORATORIES INC.
Total awards: $80,857,025 | UEI: NH3LDK8CFAK7 | DUNS: 127208879
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Federal Contractor: ABBOTT LABORATORIES
Total awards: $40,167,943 | UEI: EF9EAJ1MF6U3 | DUNS: 001307602
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Federal Contractor: ABBOTT LABORATORIES
Total awards: $40,111,022 | UEI: EF9EAJ1MF6U3 | DUNS: 001307602
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Federal Contractor: ABBOTT LABORATORIES INC.
Total awards: $14,705,571 | UEI: L3AXXYLB3V56 | DUNS: 967474896
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Federal Contractor: ABBOTT LABORATORIES INC.
Total awards: $7,987,693 | UEI: KP5EVFMHUAN1 | DUNS: 927588897
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Federal Contractor: ABBOTT LABORATORIES
Total awards: $56,921 | UEI: KG86DX52E8U5 | DUNS: 104020669
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Federal Contractor: ABBOTT LABORATORIES
Total awards: $45,000 | UEI: NZ6TR6S54JF9 | DUNS: 004283115
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