Data Composite

Recall D-0651-2024

US Class II Ongoing · initiated 2024-08-22

Recalling firm

ProRx LLC, PA

Product

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

Reason for recall

Lack of Assurance of Sterility

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