Class III
Terminated
Liptruzet (ezetimibe and atorvastin) tablets,10 mg/20 mg, a) 30 count blister (NDC 66582-321-30), b) 90 count blister (NDC 66582-321-54), Rx only, Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc, Whitehouse Station, NJ 08889
This recall has been terminated (originally issued May 14, 2014).
- Company
- Merck & Co Inc
- Recall Initiated
- January 13, 2014
- Posted
- May 14, 2014
- Recall Number
- D-1310-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 20,259 cartons
- Firm Location
- Whitehouse Station, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
This recall of LIPTRUZET is being initiated due to packaging defects. Some of the outer laminate foil pouches allowed in air and moisture, which could potentially decrease the effectiveness or change the characteristics of the product.
Distribution
Nationwide and Puerto Rico
Lot / Code Info
a) Liptruzet 10/20mg 30 count, 346353, 346354, Exp. 06/14; 351809, Exp. 07/14, 360530, Exp. 12/14. b) Liptruzet 10/20mg, 90 count, 346387, Exp. 06/14; 353185, Exp.12/14.
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