X-NAV Technologies recalls
X-NAV Technologies has 4 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 10 Apr 2024. 3 are still ongoing. The most frequent reason is device malfunction.
Total recalls4since 2016
Last 12 months0reported
Class I00% of total
Ongoing3latest 10 Apr 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why x-nav technologies is recalled
Product types
By year
Ongoing x-nav technologies recalls
3 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | X-Guide Handpiece Adaptor Sleeve recalled by X-NAV Technologies | X-NAV Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | X-Guide Handpiece Adaptor Sleeve recalled by X-NAV Technologies | X-NAV Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | X-Guide X-Mark Probe Tool -used recalled by X-NAV Technologies | X-NAV Technologies | Device Malfunction | Nationwide |
All x-nav technologies recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | X-Guide Handpiece Adaptor Sleeve recalled by X-NAV Technologies | X-NAV Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | X-Guide Handpiece Adaptor Sleeve recalled by X-NAV Technologies | X-NAV Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | X-Guide X-Mark Probe Tool -used recalled by X-NAV Technologies | X-NAV Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | X-Guide Surgical Navigation System recalled by X-NAV Technologies | X-NAV Technologies | Foreign Material | 14 states |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.