Waldemar Link GmbH & Co. KG (Mfg Site): Medical Device Recall in 2024 - (Recall #: Z-0749-2024)

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:

Link Patella Glide Resection Guide- For the implantation of the Endo-Model Knee System as part of a total knee arthroplasty procedure. Product Code: 15-2530/05

Product Classification:

Class II

Date Initiated: November 30, 2023

Date Posted: January 24, 2024

Recall Number: Z-0749-2024

Event ID: 93662

Reason for Recall:

Mislabeled: Angle and height of the device marked as L(large) corresponds to the small/medium dimensions due to a product mix-up. This may result in too little bone material resected and not fit correctly leading to extended surgery time

Status: Ongoing

Product Quantity: 1 unit

Code Information:

UDI-DI :04026575245253 Lot / Serial Number: C306165

Distribution Pattern:

US Nationwide distribution in the state of NH.

Voluntary or Mandated:

Voluntary: Firm initiated