Equi-Soft Foam — Class II drug recall D-0274-2019
Terminated recall by Ecolab Inc, reported 2018-11-28, distributed nationwide. Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
| Recall number | D-0274-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ecolab Inc, Saint Paul, MN, United States |
| Recall initiated | 2018-11-09 |
| Classified | 2018-11-20 |
| Reported by FDA | 2018-11-28 |
| Terminated | 2020-11-06 |
| Distributed | Nationwide (US) |
| Quantity | 12,540 bottles |
| Reason classes | labeling |
| NDC | 47593-0521, 47593-0521-38, 47593-0521-41, 47593-0521-56, 47593-0521-57, 47593-0521-59, 47593-0521-70 |
| Lot numbers | 06/20, 08/20, 5338HU1800, L062881 |
Product
Equi-Soft Foam, Antimicrobial Hand Soap, 0.55% Benzalkonium Chloride, 25 fl oz (750 mL), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-521-41
Reason for recall
Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
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-0274-2019. 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.