Waldemar Link GmbH & Co. KG (Mfg Site): Medical Device Recall in 2023 - (Recall #: Z-2047-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left

Product Classification:

Class II

Date Initiated: March 18, 2021

Date Posted: July 5, 2023

Recall Number: Z-2047-2023

Event ID: 92500

Reason for Recall:

The firm discovered through customer complaints that device segments may not meet specifications.

Status: Ongoing

Product Quantity: 22 units

Code Information:

Item No. 15/2973/06; UDI-DI: 04026575340736.

Distribution Pattern:

Domestic: AL, GA, IL, IN, KS, NJ, NY, and TX. Foreign: Argentina, Australia, Austria, Brazil, Finland, France, Germany, India, Italy, Spain, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated