FDAFDA · Food and drugs·Recall number D-1409-2014
Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, Inc., NDC 0008-1211-30
Published July 2, 2014 · Recall initiated: April 16, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PRISTIQ
- Manufacturer
- Pfizer Us Pharmaceutical Group
- Distributor
- Nationwide
- UPC
- 0300081210306
- Lot
- H74477, H74478, Exp. 03/16, H74479, H79766 Exp. 05/16
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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