FDAAugust 22, 2024drug

TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Lack of Assurance of Sterility

What to do

FDA enforcement status: Ongoing

Brands named

prorx

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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