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U.S. Department of Health and Human Services

Enforcement Report - Week of July 2, 2014

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Product Detail

Product Description Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, Inc., NDC 0008-1211-30
Recall Number D-1409-2014
Classification Class II
Code Info H74477, H74478, Exp. 03/16, H74479, H79766 Exp. 05/16
Product Distributed Qty 220,761 bottles
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.

Event Detail

Event Id 68001
Product Type Drugs
Status Ongoing
Recalling Firm Pfizer Us Pharmaceutical Group
City New York
State NY
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2014-04-16
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide