RecallRadar

FDA Drug recall D-1393-2019

QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102-1390 U…

On 2019-06-26 the FDA classified a Class III recall of QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102-1390 U… by Ecolab, citing incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1393-2019
ClassificationClass III
Statusterminated
Initiated2019-05-10
Published2019-06-26
Last updated2026-09-13 11:52 UTC
CompanyEcolab
DistributionUS

Product

QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102-1390 USA, NDC 47593-490-82

Reason

Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.

Identifiers

ndc47593-490-82
ndc47593-490-87
code_infoLot #: C040591, Exp 4/21

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1393-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.