Unexo Life Sciences recalls ABSORBINE jr ULTRA STRENGTH PAIN PATCH (Menthol 6.5%) due to cGMP deviations. Affected units have specific UPC codes. Consumers should contact Unexo for details.
cGMP Deviations
Unexo Life Sciences is recalling ABSORBINE jr ULTRA STRENGTH PAIN PATCH products due to manufacturing quality issues. This recall affects consumers who may have purchased these patches with specific UPC codes. The issue could lead to product failure or safety risks if not addressed.
The recall is due to cGMP deviations, which are manufacturing quality issues. These deviations could lead to product failure or safety risks if the patches do not meet quality standards. However, the specific risks are not detailed in the recall notice.
Anyone who owns or uses ABSORBINE jr ULTRA STRENGTH PAIN PATCH products with the listed UPC codes. People using these patches for pain relief are most at risk if the product fails.
Check for the product name 'ABSORBINE jr ULTRA STRENGTH PAIN PATCH' with Menthol 6.5% and one patch per box. The affected units have UPC codes 8 89476 41318 3 or 8 89476 41336 7.
Look for the UPC codes 8 89476 41318 3 or 8 89476 41336 7 on the packaging.
The recall is due to cGMP deviations, which are manufacturing quality issues. The specific risks are not detailed in the notice.
Check for the product name 'ABSORBINE jr ULTRA STRENGTH PAIN PATCH' with Menthol 6.5% and one patch per box. The affected units have UPC codes 8 89476 41318 3 or 8 89476 41336 7.
The recall notice does not specify a remedy or action for affected consumers.
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-0063-2025 — Unexo Life Sciences Unexo Life Sciences Hello, I own a Unexo Life Sciences that is covered by recall D-0063-2025 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.
