ULTRAtab Laboratories recalls APAP 32:325mg tablets with CGMP deviations. Affected lots include 18K037, 18L093, 18M006, 19A121, 19G044-006. No specific remedy stated in recall notice.
CGMP Deviations
ULTRAtab Laboratories is recalling APAP 325 mg tablets due to CGMP deviations. This means the product may not meet quality standards, though the recall does not specify a remedy or hazard severity.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the tablets do not meet safety and quality standards, but the recall does not specify how this affects safety or health.
People who purchased or use the recalled APAP 325 mg tablets from ULTRAtab Laboratories in Highland, NY. Those with the specific lot numbers listed are most at risk.
Check for the product code M700LA and lot numbers 18K037, 18L093, 18M006, 19A121, 19G044, 19G045, or 19G046 on the packaging. The product is sold as a bulk container with NDC 62959-700-00.
Look for the product code M700LA and lot numbers listed in the recall notice to confirm if your tablets are affected.
The recall notice does not state any remedy or action required.
CGMP deviations indicate failures in manufacturing quality control, but the recall does not specify how this affects safety or health.
Affected lot numbers include 18K037, 18L093, 18M006, 19A121, 19G044, 19G045, and 19G046.
We’ve drafted a message you can send ULTRAtab Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0548-2022 — ULTRAtab Laboratories ULTRAtab Laboratories Hello, I own a ULTRAtab Laboratories that is covered by recall D-0548-2022 from ULTRAtab Laboratories. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
