Home / Recalls / DermaCare, Inc. / D-035-2013

D-035-2013 Class II Terminated

Recalled by DermaCare, Inc. — Sarasota, FL

FDA drug recall D-035-2013 was initiated by DermaCare, Inc. on Sep 17, 2012 and is designated Class II. Reason for recall: Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specification. The recall status is terminated (terminated Aug 1, 2014). Affected quantity: 43,272 bottles.

Recall Details

Product Type: Drugs
Report Date: Nov 7, 2012
Initiation Date: Sep 17, 2012
Termination Date: Aug 1, 2014
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 43,272 bottles

Product Description

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.

Distribution Pattern

Nationwide

Code Information

Batch 2082-01085, 1852-01085, 2082-01213, 2152-01261, and 1782-01084

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-035-2013
openFDA file date: Oct 26, 2026
Loaded by RegDataLab: Oct 27, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.