Class I
Terminated
Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC 0008-0836-21) UPC 3 0008-0836-21 7; b) 90-count Unit of Use bottles (NDC 0008-0836-22) UPC 3 0008-0836-22 4; Rx only, Distributed by Wyeth Pharmaceuticals Inc., A subsidiary of Pfizer Inc., Philadelphia, PA 19101.
This recall has been terminated (originally issued May 28, 2014).
- Company
- Pfizer Us Pharmaceutical Group
- Recall Initiated
- March 6, 2014
- Posted
- May 28, 2014
- Recall Number
- D-1328-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 49,847 bottles
- Firm Location
- New York, NY, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule printed TKN250 which was identified as a Tikosyn (dofetilide) capsule.
Distribution
Nationwide and Puerto Rico
Lot / Code Info
Lot #: a) V130142, Exp 10/15; b) V130140, Exp 10/15
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