ULTRAtab Laboratories recalls PAIN AID ESF- tablets due to failed stability tests and inadequate lab investigations. These OTC pain relief tablets may not be safe for consumption.
CGMP Deviations: failed stability results, inadequate laboratory investigations,
ULTRAtab Laboratories is recalling PAIN AID ESF- (Acetaminophen 250mg, Aspirin 250mg, Caffeine 65mg) tablets because they failed stability tests and lab investigations. This could mean the tablets might not be safe to take.
The tablets failed stability tests and lab investigations, which means they might not be safe to consume. This could lead to potential health risks if the tablets are taken as intended.
People who bought PAIN AID ESF- tablets from bulk suppliers between 2018 and 2023 are likely affected. Those who have the specific lot numbers listed in the recall are at risk.
Check the product label for the NDC code 62959-560-00 and lot numbers like 18K070 through 20G041. These tablets come in bulk packages with corrugated boxes lined with polyethylene bags.
Look for the NDC code 62959-560-00 and lot numbers listed in the recall.
The product failed stability tests and lab investigations, which means it might not be safe to consume.
The recall does not specify a remedy, so check the product label for the NDC code and lot numbers to see if you have affected items.
The recall indicates potential safety issues due to failed stability tests, but specific health risks are not detailed.
We’ve drafted a message you can send ULTRAtab to request your refund or repair — edit it as you like.
Subject: Recall D-0327-2022 — ULTRAtab ULTRAtab Hello, I own a ULTRAtab that is covered by recall D-0327-2022 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.
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.