[Recalled] Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components — Zimmer CAS voluntarily conducted a retrospective recall
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in the placement of total knee replacement components |
|---|---|
| Brand / manufacturer | Orthosoft, Inc. dba Zimmer CAS |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1881-2017 |
| Country of notice | Canada |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 October 2011 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in Canada and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Orthosoft, Inc. dba Zimmer CAS
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.