PlainRecalls
FDA Devices Moderate Class II Ongoing

MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.

Reported: January 1, 2025 Initiated: December 2, 2024 #Z-0762-2025

Product Description

MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.

Reason for Recall

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.

Details

Recalling Firm
Moximed, Inc.
Units Affected
115
Distribution
US Nationwide distribution in the states of CA, OR, NY, OH, TX, CO, NY, VA.
Location
Fremont, CA

Frequently Asked Questions

What product was recalled?
MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.. Recalled by Moximed, Inc.. Units affected: 115.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 1, 2025. Severity: Moderate. Recall number: Z-0762-2025.