Class II
Terminated
Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, Inc., NDC 0008-1211-30
This recall has been terminated (originally issued July 2, 2014).
- Company
- Pfizer Us Pharmaceutical Group
- Recall Initiated
- April 16, 2014
- Posted
- July 2, 2014
- Recall Number
- D-1409-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 220,761 bottles
- Firm Location
- New York, NY, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq (desvenlafaxine) extended release tablets because a single Pristiq 100 mg tablet was found in a bottle of 50 mg Pristiq.
Distribution
Nationwide
Lot / Code Info
H74477, H74478, Exp. 03/16, H74479, H79766 Exp. 05/16
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