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Orthosoft, Inc. dba Zimmer CAS recalls Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Recalled May 24, 2017 · FDA recall Z-2075-2017 · Orthosoft, Inc.
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. · FDA Class III
Units
152
Sold at
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
Description
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.
Product
Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Manufacturer(s)
Orthosoft, Inc. dba Zimmer CAS
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →