Orthosoft, Inc. dba Zimmer CAS: Medical Device Recall in 2017 - (Recall #: Z-2076-2017)

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, Stereotaxic instrument

Product Classification:

Class II

Date Initiated: October 28, 2008

Date Posted: May 24, 2017

Recall Number: Z-2076-2017

Event ID: 75613

Reason for Recall:

Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack System OS Knee Universal software versions 2.2.0.82, 2.2.1.3, 2.1.6.0.2, D.54 and A.42 due to software issues resulting in erros and discrepancies .

Status: Terminated

Product Quantity: 153

Code Information:

Part Number, Lot Number/Serial Number ORTHOsoft-UniTkr- 2.2.0.82, 2.2.1.3 ORTHOsoft-UniTkr- 2.1.6.0.2 OsUniTkr (previous naming convention for ORTHOsoft-UniTkr)- D.54, A.42

Distribution Pattern:

Domestic: CA, FL, GA, IL, IN, KS, NC, NY, OH, OR, PA, RI, TN, TX, VA, WA Foreign: Canada, Australia Austria Brazil China Czech Republic France Germany Israel Italy Lebanon Luxembourg Netherlands New Zealand Spain Sweden Switzerland United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated