X-NAV recalls X-Guide X-Mark Probe Tools with missing welds that could fall into patient's mouth during use, risking aspiration. Affected units sold in 2007 with specific lot numbers.
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.
X-NAV recalls X-Guide X-Mark Probe Tools that may have a missing weld, causing the tip to fall into a patient's mouth during dental registration. This could lead to the patient aspirating or swallowing the probe tip.
The probe tool may have a missing weld connecting the tip to the shaft. If the remaining weld breaks during use, the tip could fall into the patient's mouth, potentially causing aspiration or swallowing.
Dental professionals using the X-Guide X-Mark Probe Tool for edentulous patients are most at risk. Patients receiving dental registration services with the affected tool could be impacted.
Check for the lot number 200:07010010 on the tool's packaging or label. The product was sold in 2007 with catalog number P010673.
Inspect the tool for a missing weld between the tip and shaft. If found, stop using it immediately.
The tool may have a missing weld that could cause the tip to fall into the patient's mouth during use, risking aspiration or swallowing.
Check for lot number 2007010010 on the packaging or label. The product was sold in 2007 with catalog number P010673.
Inspect the tool for a missing weld between the tip and shaft. If found, stop using it immediately.
We’ve drafted a message you can send X-NAV to request your refund or repair — edit it as you like.
Subject: Recall Z-0222-2023 — X-NAV X-NAV Hello, I own a X-NAV that is covered by recall Z-0222-2023 from X-NAV. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
