Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Semaglutide Injection Recalled by ProRx LLC Due to Lack of Assurance of Sterility
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 ProRx LLC directly.
Affected Products
Semaglutide Injection, 12.5/5mL (2.5 mg/mL), 5mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-09
Quantity: 2,809 vials
Why Was This Recalled?
Lack of Assurance of Sterility
Where Was This Sold?
This product was distributed to 2 states: TX, UT
About ProRx LLC
ProRx LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report