Zimmer, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1039-2025)

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 LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10

Product Classification:

Class II

Date Initiated: January 6, 2025

Date Posted: February 5, 2025

Recall Number: Z-1039-2025

Event ID: 96090

Reason for Recall:

It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.

Status: Ongoing

Product Quantity: 155 units

Code Information:

UDI-DI: 00889024635746; Lot Numbers:66782843 66782840 66873137

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of CA, FL, GA, KS, MO, NE, NJ, PA, TN and the countries of CHINA, INDIA, KOREA, MALAYSIA, NETHERLANDS, SINGAPORE, TAIWAN.

Voluntary or Mandated:

Voluntary: Firm initiated