# FDA recall D-0251-2022

> **Bayer Healthcare Pharmaceuticals Inc.** · Class I · drug recall initiated 2021-10-01.

## Product

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.

## 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

- **Recall number:** D-0251-2022
- **Recalling firm:** Bayer Healthcare Pharmaceuticals Inc.
- **Classification:** Class I
- **Product type:** drug
- **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

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0251-2022

## Citation

> AI Analytics. FDA recall D-0251-2022. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/D-0251-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*