Aesculap, Inc.: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Aesculap, Inc. in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

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.
Valve XS Atrium Retractor FC429R 52154756 The Valve XS Atrium Lift Retractor is used in heart surgery. The retractor is used for the temporary dilation of the left atrium in mitral valve surgery and for assistance in tricuspid valve surgery.