Conformis Recalls
34 recalls on record · August 29, 2012 to April 23, 2025 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 28, 2015Medical DevicesFDA
ConforMIS, Inc. recalls ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US)
Hazard: May contain small amounts of ethylene glycol residue
October 28, 2015Medical DevicesFDA
ConforMIS, Inc. recalls ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2, Left Lateral Catalog Number: M57220600230 (US)
Hazard: May contain small amounts of ethylene glycol residue
December 17, 2014Medical DevicesFDA
ConforMIS, Inc. recalls Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as a total knee replac
Hazard: Incorrect serial number of tibial inserts packaged in tray may result in inserts not fitting
August 29, 2012Medical DevicesFDA
Conformis Inc recalls Conformis iTotal CR-Cruciate Retaining Knee Replacement System Model Numbers: M57250600010 iTotal CR, Left Knee M5
Hazard: Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of Total CR Poly Insertion Technique