US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 15, 2024 (3 years ago)

Phenoxybenzamine Hydrochloride Capsules, USP 10mg, 100-count bottle, Rx only…

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

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.

What was recalled

Phenoxybenzamine Hydrochloride Capsules, USP 10mg, 100-count bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd, Oral Solid Dosage Unit, Ahmedabad 382213, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 60219-1502-01

Recalling firm
Amneal Pharmaceuticals of New York, LLC
NDC code
60219-1502-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0319-2024

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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