Data Foundry

Drug recalls 2019

Gel Hand Sanitizer — Class II drug recall D-1060-2019

Terminated recall by Ecolab Inc, reported 2019-04-03, distributed nationwide. Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the produ

Recall numberD-1060-2019
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmEcolab Inc, Saint Paul, MN, United States
Recall initiated2019-02-06
Classified2019-03-27
Reported by FDA2019-04-03
Terminated2022-08-11
DistributedNationwide (US)
Reason classeschemical contamination
NDC47593-0487, 47593-0487-11, 47593-0487-26, 47593-0487-31, 47593-0487-33, 47593-0487-35, 47593-0487-38, 47593-0487-41, 47593-0487-49, 47593-0487-55, 47593-0487-56, 47593-0487-65, 47593-0487-91
Expiration dates2020-08-20

Product

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 oz) bottles (NDC 47593-487-33), and c) 540 mL (18 fl oz) bottles (NDC47593-487-31) Ecolab, 370 Wabasha Street N, St. Paul, MN 55102.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1060-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.