Class II
Drug Recall: TIRZEPATIDE 20 mg/2mL (10/mg/mL), Rx Only, 2mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-01
ProRx LLC · August 22, 2024
Reason for Recall
Lack of Assurance of Sterility
Distribution
Nationwide in the USA
States Affected
NATIONWIDE
Quantity Affected
1,489 vials
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0655-2024
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.