ULTRAtab Laboratories recalls bulk acetaminophen 325mg containers due to CGMP deviations. Affected lots from Highland, NY NDC 62959-203-00 may pose quality risks.
CGMP Deviations
ULTRAtab Laboratories is recalling bulk acetaminophen 325mg containers because of manufacturing quality issues. This recall affects specific lots that may have production deviations.
CGMP deviations indicate potential quality control failures in manufacturing. These deviations could lead to inconsistent product quality or safety issues in the final product.
Healthcare facilities and pharmacies that purchased the affected bulk containers from ULTRAtab Laboratories in Highland, NY are likely affected. Staff handling these products during dispensing may be at risk.
Check for the product code L203L on the container. Affected lots include 18K012 and 19E091 from the bulk container batch.
Identify the product code L203L and lot numbers 18K012 or 19E091 on the container.
The recall indicates potential quality issues, but specific safety risks are not described in the official notice.
The official recall notice does not specify a remedy or action for affected products.
Check for product code L203L and lot numbers 18K012 or 19E091 on the container.
We’ve drafted a message you can send ULTRAtab to request your refund or repair — edit it as you like.
Subject: Recall D-0533-2022 — ULTRAtab ULTRAtab Hello, I own a ULTRAtab that is covered by recall D-0533-2022 from ULTRAtab. 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.
