US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 18, 2024 (2 years ago)

Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.

What was recalled

Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card in one carton, Rx only, Mfg by: Cadila Healthcare Ltd., Ahmedabad, India, Distributed by: Major Pharmaceutical 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, USA, NDC 0904-7075-61, UPC code: 309047075614

Recalling firm
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
NDC code
0904-7075-61
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0584-2024

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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