RemedyRepack Inc.: Drug Recall
Recall #D-0077-2023 · 12/05/2022
Class II: Risk
Recall Details
- Recall Number
- D-0077-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- RemedyRepack Inc.
- Status
- Terminated
- Date Initiated
- 12/05/2022
- Location
- Indiana, PA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9 boxes
Reason for Recall
Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
Product Description
Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816; Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC #: 70518-3493-00.
Distribution Pattern
Product was distributed to two different customers in MI.
Other Recalls by RemedyRepack Inc.
- Class II: Risk 04/22/2025
- Class II: Risk 03/24/2025
- Class II: Risk 01/24/2025
- Class II: Risk 12/02/2024
- Class II: Risk 06/26/2024
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.