Clindamycin Phosphate and Benzoyl Peroxide Gel recalled over sterility concerns
- Recall date
- December 28, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- L. Perrigo Company recalls Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel,…
- Recall number
- D-0434-2017
- FDA classification
- Class II
- Brand / firm
- L. Perrigo Company
- Sold / distributed
- Nationwide
Why it was recalled
Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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