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Recall Observatory FDA recall evidence

Device product

"****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate Pkwy***4Th floor***Sunrise, FL 33323***www.orthosensor.com***" Rx Only*** Sterile/EO***Made exclusively for Stryker Orthopaedics***. Is the graphic user interface software associated with the graphic user interface, which is loaded onto the linkstations.

Z-0122-2013

February 04, 2012

Class II

Product summary

Firm
Orthosensor
Event
Event 63081
Status
Terminated
Classification
Class II
Quantity
9
Official record key
device-enforcement:Z-0122-2013

Official wording

Reason: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface Software 1.8 (which was updated to version 1.82, validated on 02/13/12). Recall was initiated due to customer feedback which included the line of site between the knee ba lancer and the Link station was obstructed by OR metal stands or trays or the knee balancer device was placed atop of or near the metal stands or trays, interru

Code information: Version 1.82

Distribution pattern: Nationwide Distribution including the states of CA, FL, MI and NY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Ortho sensor in Sunrise, FL is recalling the Graphics User Interface Software 1.8 (which was updated to version 1.82, validated on 02/13/12). Recall was initiated due to customer feedback which included the line of site between the knee ba lancer and the Link station was obstructed by OR metal stands or trays or the knee balancer device was placed atop of or near the metal stands or trays, interru