Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Betamethasone SP PF (12 mg/mL) Recalled by US Compounding Inc Due to Lack of Assurance of Sterility; The firm is...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact US Compounding Inc directly.
Affected Products
Betamethasone SP PF (12 mg/mL), 2 mL Single Dose Vial, For IM & Regional Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3016-02
Quantity: 6,008 vials
Why Was This Recalled?
Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an impact on sterility assurance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About US Compounding Inc
US Compounding Inc has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report