Amneal Pharmaceuticals recalls specific lots of 50mg chlorproMazine tablets due to foreign micro-organism in packaging. No tablets were contaminated. Consumers should check lot numbers and contact the company for details.
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 certain lots of 50mg chlorproMazine hydrochloride tablets because packaging contained a micro-organism. This does not affect the tablets themselves but poses a risk if the packaging is handled improperly. The recall is for prescription-only medication.
The packaging for some lots of these tablets contained a micro-organism. However, the tablets themselves were not contaminated. The risk arises if the packaging is handled without proper hygiene, potentially leading to contamination of the medication.
Prescription patients who received specific lots of Amneal chlorproMazine tablets (NDC 69238-1058-1) between 2024 and 2027. Those with the highest risk are individuals handling the packaging without proper hygiene.
Check the lot numbers: AM240147, AM240148 (expiring 01/31/2027) or AM240664, AM240665 (expiring 04/30/2027). The product is a prescription-only 50mg chlorproMazine hydrochloride tablet bottle.
Look for lot numbers AM240147, AM240148 (expiring 01/31/2027) or AM240664, AM240665 (expiring 04/30/2027) on the packaging.
No, the tablets themselves were not contaminated. The micro-organism was found only in the packaging.
Check the lot numbers: AM240147, AM240148 (expiring 01/31/2027) or AM240664, AM240665 (expiring 04/30/2027).
The recall does not require immediate action for the tablets themselves. Check the lot numbers and contact Amneal Pharmaceuticals 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-0617-2025 — Amneal Amneal Hello, I own a Amneal that is covered by recall D-0617-2025 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.
