UP & UP brand — Class II drug recall D-035-2013
Terminated recall by DermaCare, Inc., reported 2012-11-07, distributed nationwide. Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specifica
| Recall number | D-035-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DermaCare, Inc., Sarasota, FL, United States |
| Recall initiated | 2012-09-17 |
| Classified | 2012-11-01 |
| Reported by FDA | 2012-11-07 |
| Terminated | 2014-08-01 |
| Distributed | Nationwide (US) |
| Quantity | 43,272 bottles |
| Reason classes | microbial contamination, sterility |
| Lot numbers | 1782-01084, 1852-01085, 2082-01085, 2082-01213, 2152-01261 |
Product
UP & UP brand, kid's foaming hand sanitizer, alcohol free, 99.9% effective against germs, Sweet s'melon, 6.7FL oz (200mL), Distributed by Target Corp., Minneapollis, MN 55403
Reason for recall
Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specification.
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-035-2013. 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.