ca_enviro
2 records
CA Environmental: ECOLAB INC — Cleanup Program Site
2009-06-02
SAN JOSE, Santa Clara County | Status: Completed - Case Closed | Agency: SAN FRANCISCO BAY RWQCB (REGION 2)
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CA Environmental: ECOLAB INC — Cleanup Program Site
1995-11-30
SAN JOSE, Santa Clara County | Status: Completed - Case Closed | Agency: SAN FRANCISCO BAY RWQCB (REGION 2)
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co_sos
1 records
courtlistener_docket
3 records
Picard v. Ecolab Inc.
2026-05-15
Federal docket 1:26-cv-12240 (mad); matched party 'Ecolab Inc.'
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Watts v. Ecolab, Inc.
2026-04-04
Federal docket 1:26-cv-03760 (ilnd); matched party 'Ecolab, Inc.'
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Watts v. Ecolab, Inc.
2026-04-04
Federal docket 1:26-cv-03759 (ilnd); matched party 'Ecolab, Inc.'
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EPA (Environmental Protection Agency)
11 records
epa_echo
16 records
EPA ECHO: ECOLAB INC.
2001-05-16
Penalty assessed: $277,953. Type: Administrative - Formal
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EPA ECHO: ECOLAB, INC.
2000-11-27
Penalty assessed: $5,000. Type: Administrative - Formal
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fda
23 records
FDA Device Recall: Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Us
2021-03-03
Class II — Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc Drapes from a single lot. A source for potential manufacturing error was identified and investigation is underway to p...
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FDA Drug Recall: Hand Sanitizer (Alcohol 80% v/v) topical solution, 55 US GAL (208 L) EcoLab Inc
2020-09-02
Class II — Discoloration and Presence of Foreign Substance
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FDA Drug Recall: QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz ca
2019-06-26
Class III — Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
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FDA Drug Recall: Express Gel Hand Sanitizer (Ethyl Alcohol 70%), 37 mL (1.25 fl oz) bottles, Ecol
2019-04-03
Class II — Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
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FDA Drug Recall: Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%), 118 mL (4 fl oz) bottles, E
2019-04-03
Class II — Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
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FDA Drug Recall: Advanced Gel Hand Sanitizer (Ethyl alcohol 62%), packaged in a) 37 mL (1.25 fl o
2019-04-03
Class II — Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
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FDA Drug Recall: Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles, E
2019-04-03
Class II — Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
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FDA Drug Recall: Gel Hand Sanitizer (Ethyl Alcohol 70%), packaged in a) 37 mL (1.25 fl oz) bott
2019-04-03
Class II — Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
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FDA Drug Recall: Equi-Soft Foam, Antimicrobial Hand Soap, 0.55% Benzalkonium Chloride, 25 fl oz (
2018-11-28
Class II — Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
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FDA Drug Recall: Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz
2018-11-28
Class II — Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
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FDA Device Recall: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx
2018-10-31
Class II — The pouches of certain lots of product may have wrinkles along the pouch seal that could result in a channel within the seal. Should there be a channel in the pouch seal it may result in a...
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FDA Device Recall: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Ster
2018-10-31
Class II — The pouches of certain lots of product may have wrinkles along the pouch seal that could result in a channel within the seal. Should there be a channel in the pouch seal it may result in a...
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FDA Device Recall: ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906, pa
2018-07-11
Class III — The incorrect IFU was shipped with the product.
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FDA Device Recall: ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, p
2018-07-11
Class III — The incorrect IFU was shipped with the product.
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FDA Device Recall: Disposable Light Handle Cover, Item Number B1-715-65. Packaged 1 device inside
2018-02-14
Class II — Sterile packaging of the disposable light handle cover may contain gaps in the seal of the pouch.
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FDA Drug Recall: Endure 400 Scrub-Stat (chlorhexidine gluconate) Foam Forming Solution, 4%, packa
2017-02-08
Class III — Subpotent Drug
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FDA Drug Recall: Scrub-Stat 4 (chlorhexidine gluconate) Foam Forming Solution, 4%, packaged in a
2016-03-16
Class III — Subpotent drug
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FDA Recall: Ecolab Inc — Class II
20140219
Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels. | Product: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL, featuring IsoSilk(R), ...
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FDA Device Recall: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL, featuring IsoSilk(R
2014-02-19
Class II — Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
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FDA Device Recall: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER, featuring IsoSilk(R), 13cm
2014-02-19
Class II — Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
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FDA Device Recall: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL, featuring IsoSilk(R),
2014-02-19
Class II — Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
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FDA Device Recall: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER, BUR HOLE COVER, 5 x 96 , REF V
2014-02-19
Class II — Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
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FDA Device Recall: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R), 5"
2014-02-19
Class II — Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
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fda_adverse
2 records
FDA AE Manufacturer: Ecolab Inc.
Drug adverse event reporter — Product: CHLORHEXIDINE GLUCONATE
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ftc_enforcement
1 records
Ecolab, Inc. / O.R. Solutions, Inc.
2011-03-02
FTC live enforcement action FY2011; matched respondent 'Ecolab, Inc.'
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lobbying
4 records
Lobbying Client: ECOLAB, INC.
Lobbied by HOLLAND & KNIGHT LLP — Manufacturer of water, hygiene and infection prevention solutions and services
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Lobbying Client: ECOLAB INC.
Lobbied by ERNST & YOUNG LLP (WASHINGTON COUNCIL ERNST & YOUNG) — Sustainability company offering water, hygiene & infection prevention solutions & services
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Lobbying Client: ECOLAB, INC.
Lobbied by HOLLAND & KNIGHT LLP — Manufacturer of water, hygiene and infection prevention solutions and services
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ny_corps
1 records
NY Corp: ECOLAB INC.
1938-01-27
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Delaware
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SEC EDGAR
1 records
sec_efts
1 records
SEC Filing: ECOLAB INC.
2024-02-23
SEC EDGAR filing — Forms: 10-K — Query: manufacturing industrial
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