ProRx LLC recalls SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84
Recalled September 11, 2024 · FDA recall D-0653-2024 · ProRx
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
1,960 vials
Sold at
Nationwide in the USA
Description
Lack of Assurance of Sterility
Product
SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04
Manufacturer(s)
ProRx LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →