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ConforMIS, Inc. recalls ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2, Right Lateral Catalog Number: M57220600240 (US)
Recalled October 28, 2015 · FDA recall Z-0140-2016 · ConforMIS
Hazard
May contain small amounts of ethylene glycol residue · FDA Class II
Units
6 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, Right Lateral Catalog Number: M57220600240 (US) M5722INT0600240 (OUS)
Manufacturer(s)
ConforMIS, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →