Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01
Reported: September 11, 2024 Initiated: August 22, 2024 #D-0650-2024
Product Description
Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- ProRx LLC
- Units Affected
- 2,490 vials
- Distribution
- Nationwide in the USA
- Location
- Exton, PA
Frequently Asked Questions
What product was recalled? ▼
Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01. Recalled by ProRx LLC. Units affected: 2,490 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-0650-2024.
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