Dermamedics Post Procedure Cream Recalled for Lack of FDA Approval
Dermamedics, L.L.C. is recalling Post Procedure Cream because the FDA determined the product is an unapproved new drug and misbranded.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II. The hazard is regulatory (unapproved/misbranded) with no reported injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Dermamedics, L.L.C. is recalling Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics Post-Laser Treatment System with a SKU number of DM 1019. The recall covers all lot codes and the product was distributed nationwide.
The FDA determined that the products are unapproved new drugs and misbranded because they were marketed without an Approved NDA/ANDA. No specific health hazards, injuries, or illnesses are reported in the source text.
Consumers should stop using the product and contact the recalling firm for further instructions.
The recalled product
- Product
- Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics Post-Laser Treatment System with a SKU number of DM 1019
- Manufacturer
- Dermamedics, L.L.C.
- Category
- Drug — Topical
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- all lot codes
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 9 recalled by Dermamedics, L.L.C. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 9 products in this recall →Related recalls
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