Clindamycin Phosphate and Benzoyl Peroxide Gel — Class II drug recall D-0434-2017
Terminated recall by L. Perrigo Company, reported 2017-01-25, distributed nationwide. Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the
| Recall number | D-0434-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | L. Perrigo Company, Allegan, MI, United States |
| Recall initiated | 2016-12-28 |
| Classified | 2017-01-17 |
| Reported by FDA | 2017-01-25 |
| Terminated | 2017-08-22 |
| Distributed | Nationwide (US) |
| Quantity | 162,534 tubes |
| Reason classes | microbial contamination, sterility |
| Pathogens | mold |
| UPC / GTIN / UDI-DI | 00345802736840 |
| NDC | 45802-0736, 45802-0736-84 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0434-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.