Class II

Drug Recall: SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04

ProRx LLC · August 22, 2024

Reason for Recall

Lack of Assurance of Sterility

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

1,960 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0653-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

ProRx LLC Drug Recall: SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04 | SafeCheck