Unexo Life Sciences recalls THERACARE MAXIMUM STRENGTH PAIN RELIEF 4% LIDOCAINE PATCHes due to cGMP deviations. Affected units have specific NDC and UPC codes. Consumers should contact Unexo for details.
cGMP Deviations
Unexo Life Sciences is recalling certain THERACARE MAXIMUM STRENGTH LIDOCAINE PATCHes because they were made under cGMP deviations. This means the patches might not be safe or effective as intended, so affected users should stop using them and contact Unexo for guidance.
The recall is due to cGMP deviations, which are quality control issues in manufacturing. These deviations could mean the patches are not safe or effective as intended, but the exact risk is not specified in the recall notice.
People who own or use the recalled THERACARE MAXIMUM STRENGTH LIDOCAINE PATCHes with the specific NDC and UPC codes listed. Those with the patches are most at risk.
Check for the NDC codes 71101-001-24 (1 patch) or 71101-001-06 (6 patches) and UPC codes 8 45717 00878 5 or 8 45717 01056 6 on the packaging.
Look for the NDC codes 71101-001-24 or 71101-001-06 and UPC codes 8 45717 00878 5 or 8 45717 01056 6 on the packaging.
The recall is due to cGMP deviations, which are quality control issues in manufacturing. The exact risk is not specified in the notice.
Check for the NDC codes 71101-001-24 (1 patch) or 71101-001-06 (6 patches) and UPC codes 8 45717 00878 5 or 8 45717 01056 6 on the packaging.
The recall notice does not specify a remedy, so contact Unexo Life Sciences directly for guidance.
We’ve drafted a message you can send Unexo Life Sciences to request your refund or repair — edit it as you like.
Subject: Recall D-0065-2025 — Unexo Life Sciences Unexo Life Sciences Hello, I own a Unexo Life Sciences that is covered by recall D-0065-2025 from Unexo Life Sciences. 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.
