MicroPort Orthopedics Inc.: Medical Device Recall in 2024 - (Recall #: Z-2244-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.

Product Classification:

Class II

Date Initiated: May 3, 2024

Date Posted: July 10, 2024

Recall Number: Z-2244-2024

Event ID: 94729

Reason for Recall:

One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3 Evolution MP Non-Porous Femoral Left in the packaging.

Status: Ongoing

Product Quantity: 40 units

Code Information:

UDI: Part EFSRN3PL: Primary DI Number M684EFSRN3PL1, Part EFSRN4PR: Primary DI Number M684EFSRN4PR1; lot Number's: MP1982097, MP1982170; Catalog Number(s): EFSRN3PL, EFSRN4PR

Distribution Pattern:

International distribution in the country of China. There is no field inventory in the United States for either lot.

Voluntary or Mandated:

Voluntary: Firm initiated