US Drug Recall Register
Class I · High risk Terminated Initiated Oct 1, 2021 (5 years ago)

Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, Labeled as (a) Product of…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Chemical Contamination: presence of benzene

What was recalled

Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, Labeled as (a) Product of Finland 20006101, (b) Product of Ireland 87022897, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, UPC 3 11017 41005 9, NDC 11523-0165-3.

Recalling firm
Bayer Healthcare Pharmaceuticals Inc.
NDC code
11523-0165-3
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0251-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Tolnaftate recalls

See all