Amneal Pharmaceuticals recalls 10mg Phenoxybenzamine Hydrochloride capsules due to potential unknown impurities. This prescription drug may pose safety risks. Consumers should contact the manufacturer for details.
Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.
Amneal Pharmaceuticals is recalling prescription Phenoxybenzamine Hydrochloride capsules (10mg, 100-count) because they contain an unknown impurity that failed quality tests. This could pose a safety risk to users, though the exact danger isn't specified in the recall.
The capsules failed quality tests for an unknown impurity. This could potentially cause health issues, but the exact risk level isn't clearly described in the recall notice.
Prescription drug users who have the specific 100-count bottle of Phenoxybenzamine Hydrochloride capsules (10mg) manufactured by Amneal Pharmaceuticals. People with medical conditions requiring this medication are most at risk.
Check for the 100-count bottle labeled 'Phenoxybenzamine Hydrochloride Capsules, USP 10mg' with lot numbers AM221153 (expiring 06/30/2024) or AM230497 (expiring 02/29/2025).
Look for the lot numbers AM221153 or AM230497 on the bottle.
The recall states the capsules failed quality tests for an unknown impurity, but the exact safety risk isn't specified.
The recall does not provide specific action steps beyond checking the product details. Contact Amneal Pharmaceuticals for further guidance.
Check the lot numbers on the bottle: AM221153 (expiring 06/30/2024) or AM230497 (expiring 02/29/2025).
We’ve drafted a message you can send Amneal Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0319-2024 — Amneal Pharmaceuticals Amneal Pharmaceuticals Hello, I own a Amneal Pharmaceuticals that is covered by recall D-0319-2024 from Amneal Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
