Reported May 28, 2014 · Terminated
Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC…
Pfizer US Pharmaceutical Group
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Pfizer Us Pharmaceutical Group · 235 E 42nd St · New York, NY · 10017-5703
Is this the product you have?
- Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC 0008-0836-21) UPC 3 0008-0836-21 7; b) 90-count Unit of Use bottles (NDC 0008-0836-22) UPC 3 0008-0836-22 4; Rx only, Distributed by Wyeth Pharmaceuticals Inc., A subsidiary of Pfizer Inc., Philadelphia, PA 19101.
- Lot codes and dates
Lot #: a) V130142Exp 10/15b) V130140Exp 10/15
- Amount recalled
- 49,847 bottles
Where it was sold
- Nationwide
- PR
Why it was recalled
Stop using this product now
Presence 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.
Using this product could cause serious injury, illness or death — stop using it now.
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