137 results
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28ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-12. The device is the power cord component for the Sesamoid Plasty CAS workstation which connects the workstation to the power mains.
FDA Recall
Terminated
·Zimmer Inc.·Product code HAW·November 2, 2009
NDI P7 Position Sensor, Stereotaxic Instrument
FDA Recall
Terminated
·Orthosoft, Inc. dba Zimmer CAS·Product code HAW·June 9, 2009
Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
FDA Recall
Terminated
·Zimmer CAS·Product code OLO·April 19, 2015
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
FDA Recall
Terminated
·Orthosoft, Inc. dba Zimmer CAS·Product code HAW·June 4, 2008
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components
FDA Recall
Terminated
·Orthosoft, Inc. dba Zimmer CAS·Product code OLO·October 6, 2011
PSI Knee System- Prosthesis, knee patellofemorotibial, semi-constrained, cemented, polymer/meal/polymer The Zimmer PSI Knee System is indicated as an orthopedic instrument system to assist in the positioning of knee replacement components.
FDA Recall
Terminated
·Zimmer CAS·Product code JWH·November 3, 2014
Navitrack System - OS Knee Universal, Stereotaxic instrument
FDA Recall
Terminated
·Orthosoft, Inc. dba Zimmer CAS·Product code HAW·October 28, 2008
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument
FDA Recall
Terminated
·Orthosoft, Inc. dba Zimmer CAS·Product code HAW·June 20, 2008
SmartTools Knee System Orthopedic Stereotaxic Instrument
FDA Recall
Terminated
·Orthosoft, Inc. dba Zimmer CAS·Product code OLO·February 20, 2017
NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
FDA Recall
Open, Classified
·Orthosoft, Inc. dba Zimmer CAS 3300-75 Queen St Montreal Canada·Product code OLO·January 7, 2022
Zimmer PERSONA Distal Valgus Alignment Guide, Nonsterile. orthopedic surgical instrument. The device sets the proper Varus/Valgus alignment of a patient's knee prior to the initial femoral resection cut being made.
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 30, 2014
Stayfuse brand intramedullary bone screw; MID 3.8 x 6 mm. Zimmer part number 00-2227-003-001.
FDA Recall
Terminated
·Pioneer Surgical Technology·Product code HWC·January 20, 2004
Spinal Concepts snap-fix polyaxial screwdriver, Manufactured by Spinal Concepts, Austin, TX, REF 781-3.
FDA Recall
Terminated
·Zimmer Inc.·Product code KWQ·December 1, 2005
Spinal Concepts polyaxial screwdriver II, Manufactured by Spinal Concepts, Austin, TX, REF 781-2.
FDA Recall
Terminated
·Zimmer Inc.·Product code KWQ·December 1, 2005
Spinal Concepts polyaxial screw driver, Manufactured by Spinal Concepts, Austin, TX, REF 781-01.
FDA Recall
Terminated
·Zimmer Inc.·Product code KWQ·December 1, 2005
Spinal Concepts polyaxial screw driver, AO, Manufactured by Spinal Concepts, Austin, TX, REF 775-01.
FDA Recall
Terminated
·Zimmer Inc.·Product code KWQ·December 1, 2005
Persona (TM) The Personalized Knee System CR Tibial Articular Surface Provisional Top Nonsterile TASP CR L 3-9 CD TOP
FDA Recall
Terminated
·Zimmer, Inc.·Product code JWH·June 10, 2013
CPT 12/14 COCR (various sizes)
FDA Recall
Terminated
·Zimmer, Inc.·Product code JDI·October 11, 2013
ASIA ONE-PIECE LAG SCREW
FDA Recall
Terminated
·Zimmer, Inc.·Product code HSB·October 11, 2013
HGP II ACETABULAR CUP BON
FDA Recall
Terminated
·Zimmer, Inc.·Product code JDI·October 11, 2013