Waldemar Link GmbH & Co. KG Recalls

17 recalls found for Waldemar Link GmbH & Co. KG. Check if any of your products are affected.

HIGHFDA DEVICE

Waldemar Link Embrace Shoulder Drill Tower Recalled After Mislabeling; 75 Units in 2026

Waldemar Link GmbH & Co. KG recalled 75 Embrace Shoulder Drill Tower devices distributed to U.S. hospitals after discovering mixed-up article numbers in the device overview. The surgical steps are correct, but the overview labeling is inaccurate. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions sent by email.

Waldemar Link GmbH & Co. KG
The surgical
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HIGHFDA DEVICE

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.

Waldemar Link GmbH & Co. KG
The surgical
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HIGHFDA DEVICE

Waldemar Link Recalls Knee Fusion Nail Due to Assembly Error

Waldemar Link GmbH & Co. KG recalled 18 units of the Endo Model Knee Fusion Nail SK on November 10, 2025. The device features a preassembled locking screw incorrectly inserted, posing a high risk of failure. Affected units were distributed in Alabama, Georgia, and Texas.

Waldemar Link GmbH & Co. KG
The device
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HIGHFDA DEVICE

Waldemar Link Recalls LinkSymphoKnee Tibial Component Over Safety Hazard

Waldemar Link GmbH & Co. KG recalled eight units of the LinkSymphoKnee Tibial Component on July 31, 2025. The recall stems from a manufacturing error involving uncoated security screws. Patients and healthcare providers should stop using the device immediately.

Waldemar Link GmbH & Co. KG
Some modular
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Brand Statistics

Total Recalls
17
Pages
1