Orthalign Recalls

2 recalls found for Orthalign. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Orthalign Lantern Knee Drill Plate Recalled for Bone-Cut Risk (2026)

Orthalign recalled 7 drill plates used with its Lantern Knee System distributed nationwide, including Utah. The parts were manufactured out of specification and can cause a bone cut up to 0.008 inch (2.8448 mm). Healthcare providers were notified by letter and instructions to stop using the devices.

Orthalign
Drill plates
Read more
Health & Personal Care
HIGH
FDA DEVICE

Orthalign Drill Plate Recall 2026 for 7 Units Over Bone-Cut Risk

Orthalign recalled 7 pegged drill plates used with the Lantern Knee System due to out-of-spec manufacturing that can cause bone cuts up to 2.8448 mm. The devices were distributed in Utah and across the United States. Healthcare providers and patients should stop using the device immediately and await recall instructions by letter.

Orthalign
Drill plates
Read more

Brand Statistics

Total Recalls
2
Pages
1