FDAFDA · Food and drugs·Recall number D-0656-2024
TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02
Published September 11, 2024 · Recall initiated: August 22, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- ProRx LLC
- Distributor
- Nationwide in the USA
- Lot
- Lot# ProRx052224, BUD 11/21/2024 ProRx061024, BUD 12/09/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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