Pfizer Us Pharmaceutical Group

FDA Regulatory Profile

Pfizer Us Pharmaceutical Group appears in FDA public data with 4 recalls — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1409-2014, Class II) was initiated on April 16, 2014.

Summary

Total Recalls
4 (1 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1409-2014Class IIPristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by WyApril 16, 2014
D-1328-2014Class IEffexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use March 6, 2014
D-1166-2014Class IIIAdvil PM Caplets, (Ibuprofen, 200 mg /Diphenhydramine citrate, 38 mg) 120 count bottle, OTC, Pfizer,February 26, 2014
D-014-2014Class IIAldactone (spironolactone) tablets, USP, 100 mg, 100-count bottles, Rx only, Distributed by G.D. SeaSeptember 4, 2013