Dermamedics Post Procedure Cream — Class II drug recall D-1487-2014
Terminated recall by Dermamedics, L.L.C., reported 2014-08-06, distributed nationwide. Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbr
| Recall number | D-1487-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dermamedics, L.L.C., Oklahoma City, OK, United States |
| Recall initiated | 2014-01-10 |
| Classified | 2014-07-29 |
| Reported by FDA | 2014-08-06 |
| Terminated | 2017-03-14 |
| Distributed | Nationwide (US) |
| Reason classes | labeling, unapproved product |
Product
Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU number of DM 1026
Reason for recall
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
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-1487-2014. 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.