CLASS II Drug recall · Reported 3 Apr 2019 · FDA Enforcement Report

Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), Ecolab recalled

Ecolab is recalling Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), Ecolab, 370 Wabasha Street N, St, distributed nationwide in the US. The recall was initiated on 6 Feb 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: HS103181, Exp. OCT 2020
Quantity recalled67 units

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1063-2019
FDA event ID
82344
Recalling firm
Ecolab, Saint Paul, MN
Classification
Class II
Status
Terminated
Recall initiated
6 Feb 2019
FDA classified
27 Mar 2019
Reported
3 Apr 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Benzene
Drug class
Hand Sanitizer

Timeline

6 Feb 2019Recall initiated by company
27 Mar 2019Classified by FDA+49 days
3 Apr 2019Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.

Product as listed by the FDA

Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-491-85

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Why was it recalled?

Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.

Which lots are affected?

Lot #: HS103181, Exp. OCT 2020

Where was it sold?

Nationwide within the United States

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 82344

This product is part of a recall event; the main page for the event is Express Gel Hand Sanitizer (Ethyl Alcohol 70%), Ecolab recalled.

More recalls from Ecolab

All 28
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IISlush + Warmer Disc Drape recalled by EcolabEcolabSterilityNationwide
DrugCLASS IIHand Sanitizer (Alcohol 80% v/v) topical solution recalled by EcolabEcolabOtherNationwide
DrugCLASS IIIQuik-care Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol) recalledQuik-careEcolabLabeling ErrorsNationwide
DrugCLASS IIGel Hand Sanitizer (Ethyl Alcohol 70%) recalled by EcolabEcolabEcolabBenzeneNationwide
DrugCLASS IIAdvanced Gel Hand Sanitizer (Ethyl alcohol 62%) recalled by EcolabAdvanced Gel Hand SanitizerEcolabBenzeneNationwide