Home / Recalls / Orthosoft, Inc. dba Zimmer CAS / Z-1868-2017

Z-1868-2017 Class II Terminated

Recalled by Orthosoft, Inc. dba Zimmer CAS — Montreal, N/A

Recall Details

Product Type
Devices
Report Date
April 26, 2017
Initiation Date
February 20, 2017
Termination Date
September 18, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
84

Product Description

SmartTools Knee System Orthopedic Stereotaxic Instrument

Reason for Recall

There has been an increase in the number of complaints regarding bent or broken Drive Pins of the Validation Tool manufactured with drawing Revision M to P

Distribution Pattern

Nationwide Distribution

Code Information

Lots: 130542A1 1405941 140146 140146-1 140147 140407A 140407A-1 140407B 140407-B-1 140860 140860-1 141035 150120 B150120 B150711

Other recalls by Orthosoft, Inc. dba Zimmer CAS

  • Z-0721-2022 Class II — NavitrackER Kit A: Knee, Model Number 20-8000-000-07, (January 7, 2022)
  • Z-1881-2017 Class II — Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Sof (October 6, 2011)
  • Z-2048-2017 Class II — NDI P7 Position Sensor, Stereotaxic Instrument (June 9, 2009)
  • Z-2076-2017 Class II — Navitrack System - OS Knee Universal, Stereotaxic instrument (October 28, 2008)
  • Z-2075-2017 Class III — Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument (June 20, 2008)
  • Z-2227-2017 Class II — Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used (June 4, 2008)