US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 1, 2017 (9 years ago)

Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count…

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

Why it was recalled

Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.

What was recalled

Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.

Recalling firm
Lucid Pharma LLC
NDC code
52343-132-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0921-2017

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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