Class II

Drug Recall: Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01

ProRx LLC · August 22, 2024

Reason for Recall

Lack of Assurance of Sterility

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

2,490 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0650-2024

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, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01 | SafeCheck