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Recall Observatory FDA recall evidence

Device product

X-Guide Handpiece Adaptor Sleeve 1, Model P010701

Z-1392-2024

March 04, 2024

Class II

Product summary

Firm
X-NAV Technologies, LLC
Event
Event 94175
Status
Ongoing
Classification
Class II
Quantity
88 units
Official record key
device-enforcement:Z-1392-2024

Official wording

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.

Code information: UDI-DI: 00817421021480; Lot: 2308010012

Distribution pattern: Worldwide distribution - US Nationwide and the countries of China, Europe, Japan.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing defect