Medique recalls extra strength headache tablets (250mg acetaminophen, 250mg aspirin, 65mg caffeine) due to FDA inspection finding manufacturing violations. Products packaged in 2-count packets with specific lot numbers.
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Medique Products is recalling extra strength headache tablets that were not manufactured under FDA-approved Current Good Manufacturing Practices. This recall follows an FDA inspection that found the products did not meet quality standards.
The FDA found that these headache tablets were not made according to current manufacturing standards. This means the products may not be safe or effective as intended, though the risk of serious harm is not specified in the recall notice.
People who purchased these headache tablets from Lil' Drug Store Products, Inc. in Cedar Rapids, IA. Those who used the tablets with the specified lot numbers are most at risk.
Check the packaging for the product name 'Extra Strength Headache' with 2-count tablets. Look for lot numbers 6492 through 7065, which expire between June 2022 and May 2023.
Look for the lot numbers listed in the recall notice: 6492 through 7065.
Reach out to Medique Products for more information about the recall and potential remedies.
The FDA found that these headache tablets were not manufactured under Current Good Manufacturing Practices during an inspection.
Check the lot number on the packaging. If it matches the recalled numbers (6492-7065), contact Medique Products for guidance.
The recall states the products were not made to FDA standards, but does not specify serious injury risks. The hazard level is low risk.
We’ve drafted a message you can send Medique Products to request your refund or repair — edit it as you like.
Subject: Recall D-0391-2022 — Medique Products Medique Products Hello, I own a Medique Products that is covered by recall D-0391-2022 from Medique Products. 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.
