FDA-Device2017-05-24Class III
Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Orthosoft, Inc. dba Zimmer CAS
Hazard
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.
Sold states
Domestic: CA, FL, GA, IL, IN, KS, MD, MN, MS, NC, NJ, NY, OR, PA, RI, SD, TN, TX, WA, WI Foreign: Germany, Spain, Czech Republic, Netherlands, Switzerland, New Zealand, Morocco, Brazil, Australia, Austria, France, Italy, Singapore, United Kingdom
Affected count
152
Manufactured in
75 Queen St #3300, Montreal, Canada
Products
Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2075-2017Don't want to check this manually?
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