Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MISHA Knee System Implant Small Recalled by Moximed, Inc. Due to Knee implant may fracture due to a supplier-related...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Moximed, Inc. directly.
Affected Products
MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.
Quantity: 115
Why Was This Recalled?
Knee implant may fracture due to a supplier-related issue with one component that has nonconforming geometry at the distal end of the absorber component that may result in a reduced wall thickness and microcracks, which may lead to new or worsening symptoms of discomfort, swelling / edema, pain or stiffness, which may necessitate removal of the device.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Moximed, Inc.
Moximed, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report