Kindest Kare Antimicrobial Foaming Handwash — Class II drug recall D-0518-2016
Terminated recall by Steris Corp, reported 2015-12-16, distributed in FL, MO, TN. Labeling: Not Elsewhere Classified; Incorrect/Undeclared Excipients: Outdated previous version of label applie
| Recall number | D-0518-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corp, Saint Louis, MO, United States |
| Recall initiated | 2015-10-27 |
| Classified | 2015-12-04 |
| Reported by FDA | 2015-12-16 |
| Terminated | 2016-07-07 |
| Distributed | FL, MO, TN |
| Reason classes | undeclared allergen, labeling |
| NDC | 00519-1452-13 |
| Lot numbers | 277120 |
| Expiration dates | 2017-06-01 |
Product
Kindest Kare Antimicrobial Foaming Handwash, Hand Soap, 0.75% Triclosan, 444 ml (15 fl oz) bottles, STERIS Corporation, 7501 Page Avenue, St. Louis, MO 63133, Reorder # 1452-RF, NDC 0519-1452-13, UPC (01)00724995 086251.
Reason for recall
Labeling: Not Elsewhere Classified; Incorrect/Undeclared Excipients: Outdated previous version of label applied to products that incorrectly states one inactive ingredient.
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-0518-2016. 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.