# FDA recall D-0434-2017

> **L. Perrigo Company** · Class II · drug recall initiated 2016-12-28.

## Product

Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel, Distributed by Perrigo, Allegan, MI --- NDC 45802-736-84, UPC 345802736840

## Reason for recall

Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0434-2017
- **Recalling firm:** L. Perrigo Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-12-28
- **Report date:** 2017-01-25
- **Termination date:** 2017-08-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allegan, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0434-2017

## Citation

> AI Analytics. FDA recall D-0434-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0434-2017. Source: US FDA. Licensed CC0.

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