Ecolab Recalls
28 recalls on record · February 19, 2014 to March 3, 2021 · Drugs, Medical Devices
Recalls by year
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21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 3, 2021Medical DevicesFDA
Ecolab Inc recalls Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover intended
Hazard: 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 prevent further recurrence. The slits may lead to a breach in the sterile barrier between fluid in the basin and the slush/warming equipment. This could pose a risk of infection to patients receiving warmed irrigation fluid or surgical slush if used during a procedure.
September 2, 2020DrugsFDA
Ecolab Inc recalls Hand Sanitizer (Alcohol 80% v/v) topical solution, 55 US GAL (208 L) EcoLab Inc 1 EcoLab Place St. Paul, MN 55102 USA, N
Hazard: Discoloration and Presence of Foreign Substance
June 26, 2019DrugsFDA
Ecolab Inc recalls QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Pa
Hazard: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
April 3, 2019DrugsFDA
Ecolab Inc recalls Express Gel Hand Sanitizer (Ethyl Alcohol 70%), 37 mL (1.25 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 5
Hazard: Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
April 3, 2019DrugsFDA
Ecolab Inc recalls Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, M
Hazard: Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
April 3, 2019DrugsFDA
Ecolab Inc recalls Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%), 118 mL (4 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, M
Hazard: Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
April 3, 2019DrugsFDA
Ecolab Inc recalls Advanced Gel Hand Sanitizer (Ethyl alcohol 62%), packaged in a) 37 mL (1.25 fl oz) bottles (NDC 47593-488-49) and b) 540
Hazard: Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
April 3, 2019DrugsFDA
Ecolab Inc recalls Gel Hand Sanitizer (Ethyl Alcohol 70%), packaged in a) 37 mL (1.25 fl oz) bottles (NDC 47593-487-49), b) 118 mL (4 fl
Hazard: Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.
November 28, 2018DrugsFDA
Ecolab Inc recalls Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St
Hazard: Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
November 28, 2018DrugsFDA
Ecolab Inc recalls Equi-Soft Foam, Antimicrobial Hand Soap, 0.55% Benzalkonium Chloride, 25 fl oz (750 mL), OTC, Ecolab, 370 Wabasha Street
Hazard: Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
October 31, 2018Medical DevicesFDA
Ecolab Inc recalls Disposable Accessory Kit, 4-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively
Hazard: 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 breach in the sterility of the product.
October 31, 2018Medical DevicesFDA
Ecolab Inc recalls Disposable Accessory Kit, 3-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively
Hazard: 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 breach in the sterility of the product.
October 31, 2018Medical DevicesFDA
Ecolab Inc recalls Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuiti
Hazard: 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 breach in the sterility of the product.
October 31, 2018Medical DevicesFDA
Ecolab Inc recalls Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Int
Hazard: 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 breach in the sterility of the product.
July 11, 2018Medical DevicesFDA
ECOLAB INC recalls ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906, packaged 1 probe cover/pouch, 25 pouches/c
Hazard: The incorrect IFU was shipped with the product.
July 11, 2018Medical DevicesFDA
ECOLAB INC recalls ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25 pouches/
Hazard: The incorrect IFU was shipped with the product.
February 14, 2018Medical DevicesFDA
Ecolab, Inc. recalls Disposable Light Handle Cover, Item Number B1-715-65. Packaged 1 device inside a peel pouch and sealed. Sealed pouches
Hazard: Sterile packaging of the disposable light handle cover may contain gaps in the seal of the pouch.
February 8, 2017DrugsFDA
Ecolab, Inc. recalls Endure 400 Scrub-Stat (chlorhexidine gluconate) Foam Forming Solution, 4%, packaged in plastic (HDPE) bottles, Over-the-
Hazard: Subpotent Drug
December 21, 2016Medical DevicesFDA
Ecolab Inc recalls Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.
Hazard: The reason for the recall is that the inner carton box of the Rolled Probe Cover PC0907NB has the incorrect expiration date (2015-10-01) on the label while the individual pouch labels and outer shipper have the correct expiration date (2018-10-01). The manufacturing date was inadvertently used as the expiration date on the inner carton box labels.
September 14, 2016Medical DevicesFDA
Ecolab Inc recalls Microtek Franz Angiography Drape with Radiation Shield, Item # RBA202, and Microtek Angiography Drape with Radiation Shi
Hazard: Ecolab is recalling 2 models of Angiography Drapes with Radiation Shields because the sterile packaging may contain small holes in the film of the pouch.
March 16, 2016DrugsFDA
Ecolab Inc recalls Scrub-Stat 4 (chlorhexidine gluconate) Foam Forming Solution, 4%, packaged in a) 800 mL Plastic (HDPE) Bottles (NDC 475
Hazard: Subpotent drug
September 30, 2015Medical DevicesFDA
Ecolab Inc recalls Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, ORS-300, ORS-301, ORS-
Hazard: The sterile packaging may contain small (less than 250 microns wide) channels in the seal of the pouch. If channels are present, the package integrity is compromised and there is a remote chance that a non-sterile drape may be used during a surgical procedure.
February 19, 2014Medical DevicesFDA
Ecolab Inc recalls Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER, BUR HOLE COVER, 5 x 96 , REF VPC0699, STERILE EO, QTY 20, Manufactured
Hazard: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
February 19, 2014Medical DevicesFDA
Ecolab Inc recalls MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL, featuring IsoSilk(R), 13cm x 249 cm, REF 3688UK, STERILE EO, Q
Hazard: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
February 19, 2014Medical DevicesFDA
Ecolab Inc recalls MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R), 5" x 98", (13cm x 249 cm), REF 3688, STERI
Hazard: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
February 19, 2014Medical DevicesFDA
Ecolab Inc recalls MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688EU
Hazard: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
February 19, 2014Medical DevicesFDA
Ecolab Inc recalls MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688
Hazard: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.
February 19, 2014Medical DevicesFDA
Ecolab Inc recalls MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688N, QTY 10
Hazard: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.