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, Stereotaxic instrument
Quantity: 153
Why Was This Recalled?
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 .
Where Was This Sold?
This product was distributed to 16 states: CA, FL, GA, IL, IN, KS, NY, NC, OH, OR, PA, RI, TN, TX, VA, WA
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