Medique recalls Physicians CARE Extra Strength pain relievers due to FDA findings of manufacturing violations. Products not made under Current Good Manufacturing Practices. Check lot numbers for affected items.
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Medique is recalling Physicians CARE Extra Strength pain relievers because they were not made following FDA manufacturing standards. This means the products may be unsafe and should not be used.
The products were found to not meet FDA manufacturing standards during an inspection. This means the pain relievers may not be safe for use and could pose health risks.
People who own or use the recalled Physicians CARE Extra Strength pain relievers are affected. Those who have the specific lot numbers listed in the recall notice are most at risk.
Check the product label for the lot numbers listed: 6151, 4360 (exp. 10/2021); 6240, 4446 (exp. 12/2021); 6331, 4484 (exp. 02/2022); 6413, 4551 (exp. 04/2022); 6699, 4679 (exp. 10/2022); 6751, 4714 (exp. 12/2022); 6855, 4750 (exp. 01/2023); 6868, 4761 (exp. 02/2023); 6899, 4776 (exp. 02/2023); 7061, 4821 (exp. 05/2023).
Look for the lot numbers listed in the recall notice on the product packaging.
The FDA found that these pain relievers were not manufactured under Current Good Manufacturing Practices during an inspection.
The recall notice does not specify a remedy, so check the lot numbers and contact Medique Products for further instructions.
The recall is due to manufacturing violations, but the specific safety risks are not detailed in the notice.
We’ve drafted a message you can send Medique Products to request your refund or repair — edit it as you like.
Subject: Recall D-0389-2022 — Medique Products Medique Products Hello, I own a Medique Products that is covered by recall D-0389-2022 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.
