EPA (Environmental Protection Agency)
2 records
fda
17 records
FDA Recall: Life Technologies Corporation — Class II
20240410
Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems exploitation of the vulnerability by a threat actor may | Product: Torrent Suite Dx Software versions 5.1...
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FDA Device Recall: Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion
2024-04-10
Class II — Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems exploitation of the vulnerability by a threat actor may allow them to alter settings, configur...
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FDA Recall: Life Technologies Corporation — Class II
20200923
COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid or inconclusive tests/false negative and potentially increasing the rete | Product: The TaqPath RT-PCR COVID-19 Kit with A...
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FDA Device Recall: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive S
2020-09-23
Class II — COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid or inconclusive tests/false negative and potentially increasing the retesting burden on customers. 2) false po...
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FDA Device Recall: Oncomine Dx Target Test DNA Control-IVD for detection of DNA and RNA isolated fr
2020-04-22
Class II — Extended Expiration Date prior to clearance
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FDA Device Recall: Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of DNA and RNA isolated
2020-04-22
Class II — Extended Expiration Date prior to clearance
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FDA Recall: Life Technologies Corporation — Class II
20191113
Component was not tested by the supplier for adventitious agents | Product: StemPro¿ MSC SFM CTS"
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FDA Device Recall: StemPro¿ MSC SFM CTS"
2019-11-13
Class II — Component was not tested by the supplier for adventitious agents
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FDA Device Recall: Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050), for In-Vitro
2018-10-24
Class II — Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
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FDA Device Recall: Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061
2018-10-24
Class II — Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
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FDA Device Recall: Gibco DPBS, calcium, magnesium, for In-Vitro Diagnostic Use SKU 14040141
2018-10-24
Class II — Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
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FDA Device Recall: Gibco Sodium Pyruvate (100 mM) SKU 11360070, for In-Vitro Diagnostic Use
2018-10-24
Class II — Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
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FDA Device Recall: GIBCO CTS AIM V Serum-Free Media (SFM), Model Number 0870112BK. Tissue and cell
2018-08-01
Class II — It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging in...
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FDA Device Recall: Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, Model Number 119651
2018-08-01
Class II — It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging in...
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FDA Device Recall: Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers
2018-08-01
Class II — It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging in...
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FDA Device Recall: Oncomine Dx Target Test User Guides and Assay Definition File, Model: A32461; UD
2018-04-11
Class II — The Oncomine Dx Target Test may report erroneous results when used off-label for samples other than non-small cell lung cancer (NSCLC) tumor specimens.
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FDA Device Recall: HSV 2 Primers, Catalog #18081020. Analyte Specific Reagent. The HSV-2 primer pai
2013-09-04
Class II — Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.
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lobbying
1 records
Lobbying Firm: LIFE TECHNOLOGIES CORPORATION
Registered lobbying firm — WASHINGTON, DC — GLOBAL BIOTECHNOLOGY TOOLS COOMPANY
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ny_corps
1 records
NY Corp: LIFE TECHNOLOGIES CORPORATION
2000-09-14
FOREIGN BUSINESS CORPORATION | County: Erie | Jurisdiction: Delaware
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USASpending
2 records
Federal Award: LIFE TECHNOLOGIES CORPORATION — $3,348,814
2024-07-03
LAB EQUIPMENT MAINTENANCE AGREEMENT
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Federal Contractor: LIFE TECHNOLOGIES CORPORATION
Total awards: $67,278,981 | UEI: EB8QTC6575E7 | DUNS: 182158873
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