Aesculap, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0492-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7

Product Classification:

Class II

Date Initiated: September 19, 2013

Date Posted: December 25, 2013

Recall Number: Z-0492-2014

Event ID: 66536

Reason for Recall:

The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.

Status: Terminated

Product Quantity: 24

Code Information:

lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597

Distribution Pattern:

Distributed in FL and MD.

Voluntary or Mandated:

Voluntary: Firm initiated