ProRx LLC recalls SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341,
Recalled September 11, 2024 · FDA recall D-0652-2024 · ProRx
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
8,396 vials
Sold at
Nationwide in the USA
Description
Lack of Assurance of Sterility
Product
SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01
Manufacturer(s)
ProRx LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →