Class II
Drug Recall: Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, 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
37 vials
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0651-2024
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.