Moximed, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0762-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 2, 2024

Date Posted: January 1, 2025

Recall Number: Z-0762-2025

Event ID: 95887

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.

Status: Ongoing

Product Quantity: 115

Code Information:

REF/UDI-DI/Lot(Expiration): 2-1001/00856047005795/23032901(29-Mar-25), 23092102(21-Sep-25), 24032601(26-Mar-26). 2-1002/00856047005801/23032902(29-Mar-25), 23092503(25-Sep-25), 24040801(8-Apr-26).

Distribution Pattern:

US Nationwide distribution in the states of CA, OR, NY, OH, TX, CO, NY, VA.

Voluntary or Mandated:

Voluntary: Firm initiated