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ABSORBINE JR PAIN RELIEVING KNEE PATCH recall

FDA recall D-0064-2025 · initiated Oct 24, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Dec 4, 2024How we research

Unexo Life Sciences Private Limited recalled ABSORBINE JR PAIN RELIEVING KNEE PATCH in Oct 2024 — an FDA Class II recall (D-0064-2025) because cGMP Deviations.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

cGMP Deviations

The manufacturing process itself

The FDA found the process itself out of compliance, usually before any defective product was identified.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

a) UPC 8 89476 41251 3 b) UPC 8 89476 41306 0

Quantity recalled: 946,080 patches

Details

Product
ABSORBINE JR PAIN RELIEVING KNEE PATCH, Camphor 7%, Menthol 7%, packaged in a) 1 patch (UPC 8 89476 41251 3) and b) 6 patches (UPC 8 89476 41306 0), Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402
Recalling company
Unexo Life Sciences Private Limited
Classification
Class II
Status
Terminated
Type
Voluntary: Firm initiated
Distribution
Nationwide in the US
Initiated
Oct 24, 2024
FDA report date
Dec 4, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was ABSORBINE JR PAIN RELIEVING KNEE PATCH recalled?
Unexo Life Sciences Private Limited recalled ABSORBINE JR PAIN RELIEVING KNEE PATCH in Oct 2024 — an FDA Class II recall (D-0064-2025) because cGMP Deviations. May cause temporary or medically reversible harm; low probability of serious harm.
Why was ABSORBINE JR PAIN RELIEVING KNEE PATCH recalled?
Per the FDA enforcement record, the reason for recall D-0064-2025 was: cGMP Deviations
Is a recalled ABSORBINE JR PAIN RELIEVING KNEE PATCH dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of ABSORBINE JR PAIN RELIEVING KNEE PATCH are affected?
Distributed: Nationwide in the US. The recall covers these lots — a) UPC 8 89476 41251 3 b) UPC 8 89476 41306 0. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0064-2025.

Source: openFDA Drug Enforcement record D-0064-2025

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