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Pfizer Us Pharmaceutical Group recalls Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals,

Recalled July 2, 2014 · FDA recall D-1409-2014 · Pfizer Us Pharmaceutical Group

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. · FDA Class II
Units
220,761 bottles
Sold at
Nationwide

Description

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.

Product
Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, Inc., NDC 0008-1211-30
Manufacturer(s)
Pfizer Us Pharmaceutical Group

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Pfizer Us Pharmaceutical Group recalls Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, | RecallWatchUSA