Ecolab Inc

Complete recall history across all FDA and CPSC categories — 26 total recalls

Ecolab Inc appears in recall records across 2 categories. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (10)

FDA drug safety enforcement actions by Ecolab Inc

Date Product Reason Class
Jul 30, 2020 Hand Sanitizer (Alcohol 80% v/v) topical solution, 55 US GAL (208 L) EcoLab I... Discoloration and Presence of Foreign Substance Class II
May 10, 2019 QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz... Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alco... Class III
Feb 6, 2019 Gel Hand Sanitizer (Ethyl Alcohol 70%), packaged in a) 37 mL (1.25 fl oz) b... Chemical Contamination: low levels of various substituted benzene (aromatic) ... Class II
Feb 6, 2019 Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles... Chemical Contamination: low levels of various substituted benzene (aromatic) ... Class II
Feb 6, 2019 Advanced Gel Hand Sanitizer (Ethyl alcohol 62%), packaged in a) 37 mL (1.25 f... Chemical Contamination: low levels of various substituted benzene (aromatic) ... Class II
Feb 6, 2019 Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%), 118 mL (4 fl oz) bottles... Chemical Contamination: low levels of various substituted benzene (aromatic) ... Class II
Feb 6, 2019 Express Gel Hand Sanitizer (Ethyl Alcohol 70%), 37 mL (1.25 fl oz) bottles, E... Chemical Contamination: low levels of various substituted benzene (aromatic) ... Class II
Nov 9, 2018 Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl... Labeling: Label mix-up - the label on the product may not match the formula ... Class II
Nov 9, 2018 Equi-Soft Foam, Antimicrobial Hand Soap, 0.55% Benzalkonium Chloride, 25 fl o... Labeling: Label mix-up - the label on the product may not match the formula ... Class II
Feb 12, 2016 Scrub-Stat 4 (chlorhexidine gluconate) Foam Forming Solution, 4%, packaged i... Subpotent drug Class III

Device Recalls (16)

FDA medical device enforcement actions by Ecolab Inc

Date Product Reason Class
Jan 11, 2021 Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product... Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc Drapes... Class II
Sep 14, 2018 Disposable Accessory Kit, 4-Arm (Box of 5) individually sealed in poly-Tyvek ... The pouches of certain lots of product may have wrinkles along the pouch seal... Class II
Sep 14, 2018 Disposable Accessory Kit, 3-Arm (Box of 5) individually sealed in poly-Tyvek ... The pouches of certain lots of product may have wrinkles along the pouch seal... Class II
Sep 14, 2018 Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx S... The pouches of certain lots of product may have wrinkles along the pouch seal... Class II
Sep 14, 2018 Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / ... The pouches of certain lots of product may have wrinkles along the pouch seal... Class II
Nov 22, 2017 ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905... The incorrect IFU was shipped with the product. Class III
Nov 22, 2017 ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906,... The incorrect IFU was shipped with the product. Class III
Nov 30, 2016 Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only. The reason for the recall is that the inner carton box of the Rolled Probe Co... Class III
Jul 14, 2016 Microtek Franz Angiography Drape with Radiation Shield, Item # RBA202, and Mi... Ecolab is recalling 2 models of Angiography Drapes with Radiation Shields bec... Class II
Aug 18, 2015 Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-10... The sterile packaging may contain small (less than 250 microns wide) channels... Class II
Jul 2, 2013 MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL, featuring IsoS... Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) t... Class II
Jul 2, 2013 MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R),... Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) t... Class II
Jul 2, 2013 Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER, BUR HOLE COVER, 5 x 96, RE... Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) t... Class II
Jul 2, 2013 MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL, featuring IsoSilk(R... Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) t... Class II
Jul 2, 2013 MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER, featuring IsoSilk(R), 1... Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) t... Class II
Jul 2, 2013 MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL, featuring IsoSil... Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) t... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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