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ConforMIS, Inc. recalls ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2, Left Lateral Catalog Number: M57220600230 (US)
Recalled October 28, 2015 · FDA recall Z-0138-2016 · ConforMIS
Hazard
May contain small amounts of ethylene glycol residue · FDA Class II
Units
7 units
Sold at
Distributed Nationwide and in Germany, Switzerland, and UK.
Description
May contain small amounts of ethylene glycol residue
Product
ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2, Left Lateral Catalog Number: M57220600230 (US) M5722INT0600230 (OUS)
Manufacturer(s)
ConforMIS, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →