Glenmark Pharmaceuticals recalls 250mg/125mg acetaminophen-ibuprofen tablets with CGMP deviations. Products sold on Amazon/Walmart with specific lot numbers and expiration dates.
CGMP Deviations
Glenmark is recalling acetaminophen and ibuprofen tablets due to manufacturing quality control issues. This recall affects specific lot numbers sold on Amazon and Walmart. The issue could lead to potential safety risks from improper production standards.
The recall is due to CGMP (Current Good Manufacturing Practices) deviations, which means the tablets were produced without following standard safety and quality controls. This could potentially lead to unsafe levels of active ingredients or contaminants in the product.
People who purchased the 144-count or 216-count packets of acetaminophen and ibuprofen tablets from Amazon or Walmart between the specified dates are affected. Those with the listed lot numbers and expiration dates are most at risk.
Check for the product name 'Acetaminophen and Ibuprofen (NSAID) Tablets, 250 mg/125 mg' on the packaging. Look for the lot numbers 17241140, 17241141, or 17241302 with expiration dates up to July 26.
Identify the product by checking the lot number and expiration date on the packaging.
The product was recalled due to CGMP deviations, which means the manufacturing process did not meet current good manufacturing practices standards.
The recall record does not specify a remedy, so you should check the product details and contact the manufacturer if you have concerns.
Look for the lot numbers 17241140, 17241141, or 17241302 with expiration dates up to July 26 on the packaging.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0347-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0347-2025 from Glenmark. 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.
