RecallRadar

FDA Drug recall D-1328-2014

Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC 0008-0836-21) UPC 3 0008-0…

On 2014-05-28 the FDA classified a Class I recall of Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (NDC 0008-0836-21) UPC 3 0008-0… by Pfizer Us Pharmaceutical Group, citing 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 identifie….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1328-2014
ClassificationClass I
Statusterminated
Initiated2014-03-06
Published2014-05-28
Last updated2026-09-13 11:51 UTC
CompanyPfizer Us Pharmaceutical Group
DistributionUS

Product

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.

Reason

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.

Identifiers

upc300080836217
upc300080836224
code_infoLot #: a) V130142, Exp 10/15; b) V130140, Exp 10/15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1328-2014%22

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