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Aesculap, Inc. recalls Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Recalled December 25, 2013 · FDA recall Z-0492-2014 · Aesculap
Hazard
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible. · FDA Class II
Units
24
Sold at
Distributed in FL and MD.
Description
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
Product
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Manufacturer(s)
Aesculap, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →