Drug recall
Navitrack System - OS Knee Universal, Stereotaxic instrument
FDA recall event 75613 · Class II · Orthosoft, Inc. dba Zimmer CAS
Key facts
| Event ID | 75613 |
|---|---|
| Recall numbers | Z-2076-2017 |
| Recalling firm | Orthosoft, Inc. dba Zimmer CAS |
| Product type | Devices |
| Products | Navitrack System - OS Knee Universal, Stereotaxic instrument |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack System OS Knee Universal software versions 2.2.0.82, 2.2.1.3, 2.1.6.0.2, D.54 and A.42 due to software issues resulting in… |
| Initiation date | Oct 28, 2008 |
| Report date | May 24, 2017 |
| Termination date | May 15, 2017 |
| City | Montreal |
| Country | Canada |
| FEI number | 3003714383 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: