Orthosoft, Inc. dba Zimmer CAS: Medical Device Recall in 2017 - (Recall #: Z-1881-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components

Product Classification:

Class II

Date Initiated: October 6, 2011

Date Posted: May 3, 2017

Recall Number: Z-1881-2017

Event ID: 75614

Reason for Recall:

Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal software ORTHOsoft-UniTkr-2.3.2.6, due to a calibration sequence crash.

Status: Terminated

Product Quantity: 105

Code Information:

Part Name: OS Knee Universal Part Number: ORTHOsoft-UniTkr-2 Affected Lot: ORTHOsoft-UniTkr-2.3.2.6

Distribution Pattern:

Worldwide Distribution - US including AZ CA CO FL GA IL IN KS MD MI MN MS OH OR PA SC SD TX VA WA and WI Internationally to Canada, Australia Austria Colombia Denmark France Germany Korea New Zealand Russia South Africa and Thailand

Voluntary or Mandated:

Voluntary: Firm initiated