TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02
Reported: September 11, 2024 Initiated: August 22, 2024 #D-0656-2024
Product Description
TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- ProRx LLC
- Units Affected
- 1,732 vials
- Distribution
- Nationwide in the USA
- Location
- Exton, PA
Frequently Asked Questions
What product was recalled? ▼
TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02. Recalled by ProRx LLC. Units affected: 1,732 vials.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 11, 2024. Severity: Moderate. Recall number: D-0656-2024.
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