Viatris: Drug Recall
Recall #D-0798-2021 · 09/13/2021
Class III: Low Risk
Recall Details
- Recall Number
- D-0798-2021
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Viatris
- Status
- Terminated
- Date Initiated
- 09/13/2021
- Location
- Morgantown, WV, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21,094
Reason for Recall
Failed Impurities/Degradation Specifications; out of specification for Related Compound
Product Description
Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 NDC 0378-3231-93
Distribution Pattern
Product was distributed nationwide.
Other Recalls by Viatris
- Class II: Risk 08/23/2021
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.