Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
X-Guide X-Mark Probe Tool -used for registering edentulous patients to Recalled by X-NAV Technologies, LLC Due to Product missing one of two welds connecting the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact X-NAV Technologies, LLC directly.
Affected Products
X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673
Quantity: 102 units
Why Was This Recalled?
Product missing one of two welds connecting the tip to the shaft, if the remaining weld breaks, it is possible that the tip could fall out during X-Mark registration and fall into the patient s mouth. In this case, the patient may aspirate or swallow the probe tip.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About X-NAV Technologies, LLC
X-NAV Technologies, LLC has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report