FDANovember 30, 2015device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

aesculap

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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. — Recall Details · AllClear