Pfizer Us Pharmaceutical Group recalls
FDA enforcement reports naming Pfizer Us Pharmaceutical Group as the recalling firm.
- Recall reports
- 4
- Class I (serious)
- 1
- Most recent report
- Jul 2, 2014
- Jul 2, 2014Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Dist…Drug · Pfizer Us Pharmaceutical GroupPresence 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.Class II
- May 28, 2014Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count…Drug · Pfizer Us Pharmaceutical GroupPresence 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.Class I
- Mar 26, 2014Advil PM Caplets, (Ibuprofen, 200 mg /Diphenhydramine citrate, 38 mg) 120 count bottle,…Drug · Pfizer Us Pharmaceutical GroupSubpotent Drug: This lot is being recalled because of out-of-specification test results for Diphenhydramine citrate.Class III
- Nov 27, 2013Aldactone (spironolactone) tablets, USP, 100 mg, 100-count bottles, Rx only, Distribute…Drug · Pfizer Us Pharmaceutical GroupMarketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting from a manufacturing site change. There is currently no approved applicat…Class II