Zimmer, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1433-2025)

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:

NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model Number 00-5962-042-10

Product Classification:

Class II

Date Initiated: February 27, 2025

Date Posted: April 2, 2025

Recall Number: Z-1433-2025

Event ID: 96400

Reason for Recall:

The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.

Status: Ongoing

Product Quantity: 76 units

Code Information:

UDI-DI: 00889024666214; Lot Numbers: 66789408, 66792792

Distribution Pattern:

Worldwide - US Nationwide distribution in the states pf CA, KS, MA, MD, ME, NE, NJ, OR, SD, and TX. The countries of Canada, China, India, Netherlands, Singapore.

Voluntary or Mandated:

Voluntary: Firm initiated