Low risk — use of or exposure to this product is not likely to cause 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
Quantity: 152
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 20 states: CA, FL, GA, IL, IN, KS, MD, MN, MS, NJ, NY, NC, OR, PA, RI, SD, TN, TX, 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