Class II Recall

Bayer Healthcare Pharmaceuticals Inc.

Product
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 59036 7, NDC 11523-0010-1.
Reason
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Classification
Class II
Status
Terminated
Lot
Lot # TN005K4, EXP 4/30/2022; TN005K8, EXP 6/30/2022
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Bayer Healthcare Pharmaceuticals Inc. — Class II Recall | MedicineWatch US