FDA recall D-0249-2022

Product

Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 58720 6, NDC 11523-0010-2.

Reason for recall

Chemical Contamination: presence of benzene

Distribution

Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.

Key facts

Status

Terminated

Initiation date

2021-10-01

Report date

2021-11-24

Termination date

2023-06-26

Voluntary/Mandated

Voluntary: Firm initiated

Location

Whippany, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0249-2022