Waldemar Link GmbH & Co. KG (Mfg Site)

Devices and FDA recall records listed on MedWatcher for Waldemar Link GmbH & Co. KG (Mfg Site).

What MedWatcher tracks

This page covers the devices and recall records listed below, not the complete product catalogue or recall history. A recall may apply only to specific models, lots, or serial numbers.

Tracked devices: 0
Recall records: 3
Source records last checked: Oct 28, 2026

Manufacturer names

Device and manufacturer names are linked using official product, UDI, or FDA records. The source links below show the supporting information.

Official records may use a legal name, brand, division, or shortened name. Similar names do not necessarily refer to the same manufacturer.

Waldemar Link GmbH & Co. KG (Mfg Site)Source-name variantOfficial source (opens in a new tab)

Sources used for this page

U.S. Food and Drug AdministrationFDA medical device recall event 97971Last checked Aug 16, 2026 U.S. Food and Drug AdministrationFDA medical device recall event 98342Last checked Aug 16, 2026

Recent recall records

Class II recallOngoing

Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16 recall — FDA event 99405

The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be…

FDA · FDA event 99405Posted Aug 11, 2026

Class II recallOngoing

Endo-Model SL Connection Component incl recall — FDA event 98342

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

FDA · FDA event 98342Posted Mar 10, 2026

Class II recallOngoing

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.

FDA · FDA event 97971Posted Dec 9, 2025

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Recent recall records

Class II recallOngoing

Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16 recall — FDA event 99405

FDA · FDA event 99405Posted Aug 11, 2026

Class II recallOngoing

Endo-Model SL Connection Component incl recall — FDA event 98342

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

FDA · FDA event 98342Posted Mar 10, 2026

Class II recallOngoing

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.

FDA · FDA event 97971Posted Dec 9, 2025

Waldemar Link GmbH & Co. KG (Mfg Site)

Follow Waldemar Link GmbH & Co. KG (Mfg Site)

What MedWatcher tracks

Manufacturer names

Sources used for this page

Recent recall records

Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16 recall — FDA event 99405

Endo-Model SL Connection Component incl recall — FDA event 98342

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

Waldemar Link GmbH & Co. KG (Mfg Site)

Follow Waldemar Link GmbH & Co. KG (Mfg Site)

What MedWatcher tracks

Manufacturer names

Sources used for this page

Recent recall records

Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16 recall — FDA event 99405

Endo-Model SL Connection Component incl recall — FDA event 98342

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971