QUIK-CARE Aerosol Foam Hand Sanitizer — Class III drug recall D-1393-2019
Terminated recall by Ecolab Inc, reported 2019-06-26, distributed nationwide. Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
| Recall number | D-1393-2019 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ecolab Inc, Saint Paul, MN, United States |
| Recall initiated | 2019-05-10 |
| Classified | 2019-06-18 |
| Reported by FDA | 2019-06-26 |
| Terminated | 2022-09-17 |
| Distributed | Nationwide (US) |
| Quantity | 183 cases |
| Reason classes | undeclared allergen |
| NDC | 47593-0490, 47593-0490-82, 47593-0490-87 |
| Lot numbers | 4/21, C040591 |
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 for recall
Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
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-1393-2019. 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.