CLENZIderm M — Class II drug recall D-916-2013
Terminated recall by Medicis Pharmaceutical Corp, reported 2013-08-28, distributed nationwide. cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottl
| Recall number | D-916-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medicis Pharmaceutical Corp, Scottsdale, AZ, United States |
| Recall initiated | 2013-05-01 |
| Classified | 2013-08-22 |
| Reported by FDA | 2013-08-28 |
| Terminated | 2014-04-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB, MX, RU, UA |
| Reason classes | labeling, cgmp |
| Lot numbers | 11J1075, 11L1074 |
Product
CLENZIderm M.D. Acne Therapeutic System Normal to Oily Skin kit, Distributed by OMP, Inc., Long Beach, CA 90806, Kit is comprised of: Daily Care Foaming Cleanser (Salicylic Acid 2%) NDC 62032-111; Pore Therapy (Salicylic Acid 2%) NDC 62032-110 and Therapeutic Lotion (Benzoyl Peroxide 5%) NDC 562032-113). Product under recall is the Pore Therapy (Salicylic Acid 2%), NDC 62032-110.
Reason for recall
cGMP Deviations; during the production process, CLENZIderm M.D. Daily Foam Cleanser was filled into some bottles labeled as CLENZIderm M.D. Pore Therapy
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-916-2013. 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.