AvKARE: Drug Recall
Recall #D-0529-2025 · 06/26/2025
Class III: Low Risk
Recall Details
- Recall Number
- D-0529-2025
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- AvKARE
- Status
- Ongoing
- Date Initiated
- 06/26/2025
- Location
- Pulaski, TN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 8,573 bottles
Reason for Recall
Failed Impurity/Degradation Specifications
Product Description
Pitavastatin Tablets, 2 mg, 90 Tablets per bottle, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 42291-906-90
Distribution Pattern
Nationwide in the USA
Other Recalls by AvKARE
- Class II: Risk 12/31/2025
- Class II: Risk 09/02/2025
- Class II: Risk 08/25/2025
- Class II: Risk 08/25/2025
- Class III: Low Risk 06/26/2025
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.