Waldemar Link GmbH & Co. KG (Mfg Site): Medical Device Recall in 2025 - (Recall #: Z-2541-2025)

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:

LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. REF Number: 880-100/50

Product Classification:

Class II

Date Initiated: July 31, 2025

Date Posted: September 17, 2025

Recall Number: Z-2541-2025

Event ID: 97383

Reason for Recall:

Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.

Status: Ongoing

Product Quantity: 8 units

Code Information:

REF Number: 880-100/50. UDI-DI: 04026575251278. Serial Numbers: 210125/2259, 210125/2262, 210125/2268, 210125/2260, 210125/2264, 210125/2270, 210125/2272, 210125/2273.

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of CO, IN, NJ, TX and the countries of Germany and Italy.

Voluntary or Mandated:

Voluntary: Firm initiated