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...
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
About Orthosoft, Inc. dba Zimmer CAS
Orthosoft, Inc. dba Zimmer CAS has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report