Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Navitrack System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer CAS Due to Zimmer CAS voluntarily conducted a retrospective recall of...

Date: October 6, 2011
Company: Orthosoft, Inc. dba Zimmer CAS
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Orthosoft, Inc. dba Zimmer CAS directly.

Affected Products

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

Quantity: 105

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 21 states: AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MS, OH, OR, PA, SC, SD, TX, VA, WA, WI

Affected (21 states)Not affected

About Orthosoft, Inc. dba Zimmer CAS

Orthosoft, Inc. dba Zimmer CAS has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report