Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02
Reported: September 11, 2024 Initiated: August 22, 2024 #D-0654-2024
Product Description
Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- ProRx LLC
- Units Affected
- 500 vials
- Distribution
- Nationwide in the USA
- Location
- Exton, PA
Frequently Asked Questions
What product was recalled? ▼
Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02. Recalled by ProRx LLC. Units affected: 500 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-0654-2024.
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