Class II Recall

ProRx LLC

Product
Semaglutide Injection, 8mg/3.2mL (2.5 mg/mL), 3.2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-09
Reason
Lack of Assurance of Sterility
Classification
Class II
Status
Ongoing
Lot
Lot Prorx051525-1, Prorx051525-2, Prorx051525-3 and Prorx051525-4
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
ProRx LLC — Class II Recall | MedicineWatch US