US Drug Recall Register
Class I · High risk Terminated Initiated Mar 6, 2014 (13 years ago)

Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Foreign Tablets/Capsules: report of a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule was found in a bottle of Effexor XR (venlafaxine HCl) 150 mg capsules that was packaged in the same packaging campaign as the recalled lot

What was recalled

Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0182-2, UPC 3 59762-0182-2 9.

Recalling firm
Greenstone Llc
NDC code
59762-0182-2
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1361-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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