Orthosoft, Inc. dba Zimmer CAS: Medical Device Recalls in 2017

According to to data from the FDA, there were 6 medical device recalls made by Orthosoft, Inc. dba Zimmer CAS in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
• SmartTools Knee System Orthopedic Stereotaxic Instrument
• Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components
• Navitrack System - OS Knee Universal, Stereotaxic instrument
• Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the tracking software as part of the software based navigation systems. The affected Sesamoid Plasty components are the central structural column and its base that hold up the computer and the tracking camera on the Sesamoid Plasty workstation. They are also designed to be disassembled such that the column can be folded onto itself for ease of transport after use. This is a retrospective recall report for a removal initiated on 17 June 2008
• NDI P7 Position Sensor, Stereotaxic Instrument