Class II — X-NAV Technologies, LLC
| Recalling firm | X-NAV Technologies, LLC. |
|---|---|
| Registered facility | X-NAV TECHNOLOGIES, LLC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The Handpiece Adaptor may have a manufacturing defect causing incorrect geometry. The incorrect geometry in turn causes the Handpiece Adaptor to not fit onto the doctor's dental handpiece. |
| Product | X-Guide Handpiece Adaptor Sleeve 1, Model P010701 |
| Quantity | 88 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of China, Europe, Japan. |
| Initiated | 2024-03-04 |
| Classified | 2024-03-29 |
| Recall number | Z-1392-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — X-NAV Technologies, LLC (Z-1392-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94175/
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