Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap Inc. US has initiated a recall on...
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, Inc. directly.
Affected Products
Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint.
Quantity: 1232
Why Was This Recalled?
Aesculap Inc. US has initiated a recall on Tibial and Femur extension sterile pressfit stem implant packaging that are used for Columbus Revision/Enduro Knee Implants because it is labeled as Cementless. US product is indicated in the US for use with Bone Cement only.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aesculap, Inc.
Aesculap, Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report