Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
What was recalled
Dermamedics Post Procedure Cream, 1 ounce containers which were distributed with a SKU number of DM 1026
- Recalling firm
- Dermamedics, L.L.C.
- Origin
- OK, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1487-2014
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
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