Provepharm Inc.: Drug Recall
Recall #D-0230-2025 · 01/21/2025
Class I: Dangerous
Recall Details
- Recall Number
- D-0230-2025
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Provepharm Inc.
- Status
- Ongoing
- Date Initiated
- 01/21/2025
- Location
- Collegeville, PA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 24640 vials
Reason for Recall
Presence of Particulate Matter.
Product Description
Phenylephrine HCl Injection, USP 100 mg/10 mL (10 mg/mL) vials, Rx only, Pharmacy Bulk Package (supplied as a single unit), Dist. by: Provepharm, Inc., Collegeville, PA 19426
Distribution Pattern
Nationwide in the U.S.
Other Recalls by Provepharm Inc.
- Class II: Risk 11/22/2024
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.