ULTRAtab Laboratories recalls specific lots of HPC tablets due to CGMP deviations. These tablets contain acetaminophen, aspirin, caffeine, and salicylamide. Consumers should check product codes and lots for affected batches.
CGMP Deviations
ULTRAtab Laboratories is recalling certain lots of HPC tablets that contain acetaminophen, aspirin, caffeine, and salicylamide. The recall is due to CGMP deviations, which means the manufacturing process did not meet quality standards. This could potentially affect the safety and effectiveness of the medication.
CGMP deviations refer to failures in the manufacturing process that could lead to unsafe or ineffective medication. This means the tablets might not contain the correct ingredients or could have impurities that affect safety and effectiveness.
People who own or use the recalled HPC tablets with the specific product codes and lots listed in the recall notice are affected. Those taking the medication for pain or fever may be at risk if they have the affected batches.
Check the product code (L242SRC, L242L, L242PA, L242N) and lot numbers (e.g., 18K086, 18L009) on the packaging. The product is sold in bulk containers with the brand ULTRAtab.
Look for the product code and lot number on the packaging to confirm if it is affected.
The hazard is CGMP deviations, which means the manufacturing process did not meet quality standards, potentially affecting the safety and effectiveness of the medication.
Check the product code (L242SRC, L242L, L242PA, L242N) and lot numbers (e.g., 18K086, 18L009) on the packaging.
The recall does not specify a remedy, so check with ULTRAtab Laboratories for further instructions.
We’ve drafted a message you can send ULTRAtab to request your refund or repair — edit it as you like.
Subject: Recall D-0538-2022 — ULTRAtab ULTRAtab Hello, I own a ULTRAtab that is covered by recall D-0538-2022 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.
