Drug recall D-0581-2021
Product
Desvenlafaxine Extended-Release Tablets 25 mg 30 Tablets Rx Only NDC 0591-4060-30 Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
1399650A
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 57 bottles
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Desvenlafaxine – drug information
- NDC 0591-3659 Desvenlafaxine · Desvenlafaxine Succinate 50 mg/1 · Actavis Pharma, Inc.
- NDC 0591-3660 Desvenlafaxine · Desvenlafaxine Succinate 100 mg/1 · Actavis Pharma, Inc.
- NDC 0591-4060 Desvenlafaxine · Desvenlafaxine Succinate 25 mg/1 · Actavis Pharma, Inc.