ProRx LLC: Drug Recall
Recall #D-0653-2024 · 08/22/2024
Class II: Risk
Recall Details
- Recall Number
- D-0653-2024
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- ProRx LLC
- Status
- Ongoing
- Date Initiated
- 08/22/2024
- Location
- Exton, PA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,960 vials
Reason for Recall
Lack of Assurance of Sterility
Product Description
SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04
Distribution Pattern
Nationwide in the USA
Other Recalls by ProRx LLC
- Class II: Risk 10/15/2025
- Class II: Risk 10/15/2025
- Class II: Risk 10/15/2025
- Class II: Risk 10/15/2025
- Class II: Risk 10/15/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.