Waldemar Link Recalls

6 recalls found for Waldemar Link. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model Replacement Plateau Recalled for 7 Units Worldwide (2026)

Waldemar Link recalled 7 Endo-Model Replacement Plateau devices distributed worldwide, including New Jersey. The recall targets an implant component where a bushing could detach from the screw shaft after a longitudinal fracture. Healthcare providers and patients should stop using the device and follow recall instructions provided by the manufacturer.

Waldemar Link
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Recalled 3 Endo-Model Replacement Plateau Implants (2026)

Waldemar Link recalled 3 Endo-Model Replacement Plateau implants distributed worldwide, including New Jersey. The devices carry a risk that a bushing could detach from the plateau screw shaft due to a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

Waldemar Link
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model Replacement Plateau Recall 4 Units (15-8030/12) in 2026

Waldemar Link GmbH & Co. KG recalled 4 Endo-Model Replacement Plateau devices, Item Number 15-8030/12, sold to hospitals and clinics worldwide including New Jersey. The defect involves a plateau screw, where a longitudinal fracture could cause the bushing to detach from the screw shaft. Healthcare providers and patients should stop using the device immediately and follow recall instructions from/​

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The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model SL Implant Component Recalled for Detachment Risk (2026)

Waldemar Link recalled 44 Endo-Model SL implant components sold through multiple distributors worldwide, including 1 unit in the United States. The bushing could detach from the screw shaft because of a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Waldemar Link for returns or replacements.

Waldemar Link
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model SL Connection Component Recalled for 31 Units (2026)

Waldemar Link recalled 31 Endo-Model SL Connection Components incl. PE-Plateau sold worldwide, including New Jersey. The device bears a risk that the bushing could detach from the screw shaft due to a longitudinal fracture. Clinicians and patients should stop using the device immediately and follow manufacturer instructions.

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Brand Statistics

Total Recalls
6
Pages
1

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