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ConforMIS, Inc. recalls Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as a total knee replac
Recalled December 17, 2014 · FDA recall Z-0581-2015 · ConforMIS
Hazard
Incorrect serial number of tibial inserts packaged in tray may result in inserts not fitting · FDA Class II
Units
1 unit
Sold at
Distributed to IN.
Description
Incorrect serial number of tibial inserts packaged in tray may result in inserts not fitting
Product
Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as a total knee replacement in patients with knee joint pain and disability.
Manufacturer(s)
ConforMIS, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →