Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Recalled by KaVo Dental Technologies LLC Due to The sensor's look up calibration files were incorrectly...

Date: April 29, 2019
Company: KaVo Dental Technologies LLC
Status: Terminated
Source: FDA (Device)

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 KaVo Dental Technologies LLC directly.

Affected Products

DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is intended to acquire dental intraoral radiographic images. The DEXIS / KaVo sensor shall be operated by healthcare professionals, who are educated and competent to perform the acquisition of dental intra-oral radiographs. The DEXIS / KaVo sensor can be used either in combination with special positioning devices to facilitate positioning and alignment with the x-ray beam or it may also be positioned by hand with the assistance of the patient.

Quantity: 211 devices

Why Was This Recalled?

The sensor's look up calibration files were incorrectly programmed during manufacturing, which can result in the reduction of image quality.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About KaVo Dental Technologies LLC

KaVo Dental Technologies LLC has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report