Bayer Healthcare Pharmaceuticals Inc. recalls Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, Labeled as (a) Product of Finland 20006101, (b) Product…
- Recall date
- October 1, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0251-2022
- FDA classification
- Class I
- Brand / firm
- Bayer Healthcare Pharmaceuticals Inc.
- Sold / distributed
- Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.
Why it was recalled
Chemical Contamination: presence of benzene
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
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.
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