Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Recalled by Aesculap Implant Systems Due to During an internal quality inspection, the tibia plateau...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aesculap Implant Systems directly.
Affected Products
Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Columbus Revision Knee System is indicated for use in reconstruction of the diseased knee joint caused by osteoarthritis, rheumatoid arthritis, post-traumatic arthritis, the need to revise failed arthroplastics or osteotomies where pain, deformity or dysfunction persist, and for patients suffering from correctable valgus or varus deformity and moderate flexion contracture
Quantity: 8
Why Was This Recalled?
During an internal quality inspection, the tibia plateau was found to be out of specification. There is a potential for misalignment between the tibia plateau and attachment of the extension stem.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aesculap Implant Systems
Aesculap Implant Systems has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report