X-NAV Technologies, LLC

Complete recall history across all FDA and CPSC categories — 4 total recalls

X-NAV Technologies, LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (4)

FDA medical device enforcement actions by X-NAV Technologies, LLC

Date Product Reason Class
Mar 4, 2024 X-Guide Handpiece Adaptor Sleeve 1, Model P010701 The Handpiece Adaptor may have a manufacturing defect causing incorrect geome... Class II
Mar 4, 2024 X-Guide Handpiece Adaptor Sleeve 3, Model P010727 The Handpiece Adaptor may have a manufacturing defect causing incorrect geome... Class II
Sep 28, 2022 X-Guide X-Mark Probe Tool -used for registering edentulous patients to the so... Product missing one of two welds connecting the tip to the shaft, if the rema... Class II
Feb 23, 2016 X-Guide Surgical Navigation System, X-Clip Bulk Kit The X-Guide Surgical N... The X-Guide system utilizes an X-Clip (PN P007665) which contains fiducials t... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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