Akorn, Inc: Drug Recall
Recall #D-1361-2022 · 08/01/2022
Class II: Risk
Recall Details
- Recall Number
- D-1361-2022
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Akorn, Inc
- Status
- Ongoing
- Date Initiated
- 08/01/2022
- Location
- Gurnee, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14,712 bottles
Reason for Recall
Defective Container: Product has incomplete induction seals.
Product Description
PrednisoLONE Oral Solution USP, 15 mg per 5 mL, 240 ml bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC: 50383-042-24
Distribution Pattern
Nationwide USA
Other Recalls by Akorn, Inc
- Class II: Risk 04/26/2023
- Class II: Risk 04/26/2023
- Class II: Risk 04/26/2023
- Class II: Risk 04/26/2023
- Class II: Risk 04/26/2023
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.