US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 3, 2016 (10 years ago)

Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx…

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

Why it was recalled

Failed Dissolution Specifications: Out-of-specification results in retained sample.

What was recalled

Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90

Recalling firm
Golden State Medical Supply Inc.
NDC code
60429-122-90
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1459-2016

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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