Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1881-2017 — Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components

U.S. FDA — Device Enforcement · Canada · 2011-10-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1881-2017
Date of alert
2011-10-06
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Orthosoft, Inc. dba Zimmer CAS
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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