Amerisource Health recalls chlorpromazine hydrochloride tablets (50mg) with specific lots due to a microorganism found in packaging. No tablets were contaminated. Consumers should contact the manufacturer for details.
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Amerisource Health is recalling certain chlorpromazine hydrochloride tablets (50mg) because a microorganism was detected in the packaging material for specific lots. This does not affect the tablets themselves but poses a risk if the packaging is compromised.
A microorganism was found in the auxiliary polyester coil used for packaging, but no microorganisms were detected on the tablets themselves. The risk arises if the packaging is damaged or compromised, potentially leading to contamination.
Prescription patients who received the recalled lots (1022159, 1023299, 1024057) of chlorpromazine tablets. Patients using these specific lots are most at risk.
Check the lot numbers on the packaging: 1022159 (expires 12/31/2026), 1023299 (expires 03/31/2027), or 1024057 (expires 04/30/2027). The product is a prescription-only chlorpromazine hydrochloride tablet blister pack.
Look for lot numbers 1022159, 1023299, or 1024057 on the packaging to identify affected products.
No, the microorganism was only found in the packaging material, not on the tablets themselves.
The recall record does not specify a remedy, so contact Amerisource Health directly for further instructions.
Check the lot numbers on the packaging: 1022159 (expires 12/31/2026), 1023299 (expires 03/31/2027), or 1024057 (expires 04/30/2027).
We’ve drafted a message you can send Amerisource Health to request your refund or repair — edit it as you like.
Subject: Recall D-0648-2025 — Amerisource Health Amerisource Health Hello, I own a Amerisource Health that is covered by recall D-0648-2025 from Amerisource Health. 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.
