Fagron, Inc: Drug Recall
Recall #D-0863-2022 · 03/04/2022
Class III: Low Risk
Recall Details
- Recall Number
- D-0863-2022
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Fagron, Inc
- Status
- Terminated
- Date Initiated
- 03/04/2022
- Location
- Saint Paul, MN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 53 containers
Reason for Recall
Subpotent Drug
Product Description
Nandrolone Decanoate, USP, 500 g per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-05
Distribution Pattern
Nationwide within the USA
Other Recalls by Fagron, Inc
- Class II: Risk 12/11/2023
- Class II: Risk 12/11/2023
- Class II: Risk 12/11/2023
- Class II: Risk 12/11/2023
- Class III: Low Risk 03/04/2022
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.