Navitrack¿ System — Class III medical device recall Z-2075-2017
Terminated recall by Orthosoft, Inc. dba Zimmer CAS, reported 2017-05-24, distributed in CA, FL, GA, IL, IN, KS, MD, MN…. ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal, due to so
| Recall number | Z-2075-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Orthosoft, Inc. dba Zimmer CAS, Montreal, Canada |
| Recall initiated | 2008-06-20 |
| Classified | 2017-05-12 |
| Reported by FDA | 2017-05-24 |
| Terminated | 2017-05-15 |
| Distributed | CA, FL, GA, IL, IN, KS, MD, MN, MS, NC, NJ, NY, OR, PA, RI, SD, TN, TX, WA, WI |
| Countries outside the US | AT, AU, BR, CH, CZ, DE, ES, FR, GB, IT, MA, NL, NZ, SG |
| Quantity | 152 |
| Reason classes | software |
Product
Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2075-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.