Amneal recalls 25mg chlorproMAZINE tablets with foreign micro-organism in packaging. No tablets were contaminated. Affected lots: AM240617, AM240618 (expiring 04/30/2027).
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Amneal Pharmaceuticals is recalling 25mg chlorproMAZINE hydrochloride tablets that may have a foreign micro-organism in their packaging. This does not affect the tablets themselves, but the packaging issue could pose a risk if the packaging is compromised.
A specific type of packaging material used for the tablets contained a micro-organism. However, no micro-organism was found on the actual tablets themselves. The risk comes from potential contamination if the packaging is damaged or compromised.
Prescription patients who received the specific lots (AM240617 or AM240618) of 25mg chlorproMAZINE tablets from Amneal. Patients with the correct NDC number (69238-1056-1) and expiration date (04/30/2027) are most at risk.
Check for the lot numbers AM240617 or AM240618 on the packaging. The tablets are 25mg, 100-count bottles with NDC 69238-1056-1 and expire 04/30/2027.
Look for lot numbers AM240617 or AM240618 on the packaging.
No micro-organism was detected on any tablets. The issue is with the packaging material.
No, the tablets themselves are safe. Only the packaging may have a foreign substance.
Check the packaging for lot numbers AM240617 or AM240618. If you have these, contact Amneal for further instructions.
We’ve drafted a message you can send Amneal to request your refund or repair — edit it as you like.
Subject: Recall D-0616-2025 — Amneal Amneal Hello, I own a Amneal that is covered by recall D-0616-2025 from Amneal. 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.
