Orthosoft, Inc. dba Zimmer CAS: Medical Device Recall in 2017 - (Recall #: Z-2075-2017)

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

Product Classification:

Class III

Date Initiated: June 20, 2008

Date Posted: May 24, 2017

Recall Number: Z-2075-2017

Event ID: 75612

Reason for Recall:

ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal, due to software anomalies which were corrected with a new revision in version 2.2.1.3.

Status: Terminated

Product Quantity: 152

Code Information:

Product Name: Orthosoft Universal TKR (software application) Product Number: ORTHOsoft-UniTkr-2 Affected Lot #: Software release version ORTHOsoft-UniTkr-2.2.0.82

Distribution Pattern:

Domestic: CA, FL, GA, IL, IN, KS, MD, MN, MS, NC, NJ, NY, OR, PA, RI, SD, TN, TX, WA, WI Foreign: Germany, Spain, Czech Republic, Netherlands, Switzerland, New Zealand, Morocco, Brazil, Australia, Austria, France, Italy, Singapore, United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated