Synergy Rx Recalls Benzoyl Peroxide and Clindamycin Due to Sterility Concerns
Synergy Rx is recalling Benzoyl Peroxide 5% Clindamycin 1.2% due to lack of assurance of sterility and CGMP deviations.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric for drug recalls involving potential health risks.
Plain-English summary
Synergy Rx is recalling Benzoyl Peroxide 5% Clindamycin 1.2%, a prescription-only topical medication. The recall was initiated because the product lacks assurance of sterility and the manufacturer has Current Good Manufacturing Practice (CGMP) deviations.
The recall covers all lots of the product. The medication was distributed nationwide within the United States.
Consumers with this product should stop using it and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- BENZOYL PEROXIDE 5% CLINDAMYCIN 1.2%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
- Manufacturer
- Synergy Rx
- Category
- Drug — Topical Antibiotic
- Hazard
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 Lots
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 81 recalled by Synergy Rx 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.
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