Reported Oct 8, 2014 · Terminated

eXpertDC intraoral x-ray, models

Gendex Corp.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Gendex Corp · 2800 Crystal Dr · Hatfield, PA · 19440-1944

Is this the product you have?

Models

10 of 10 products

Products covered by this recall
#Product as published
1eXpert DC, NA, 75 Inch reach
2eXpert DC, NA, 65 Inch reach
3eXpert DC, CN, 55 Inch reach
4eXpert DC, WW, 75 Inch reach
5eXpert DC, WW, 65 Inch reach
6eXpert DC, WW, 55 Inch reach
7OEM Arm Assembly w/o cables
8Assy, Articulated Arm & Tubehead, eDC
9and Assy, Articulated Arm & Tubehead, 765DC
10with multiple part numbers and serial numbers: see distribution list for these details.
Amount recalled
651

Where it was sold

  • Nationwide

Why it was recalled

Two (2) failures of the spring link components within the articulated arm assembly. The spring links broke during normal assembly process for the articulated arm during first cycle of the arm, prior to the 14lb tube head (full load) being installed onto the assembled articulated arm.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Gendex Corp. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 24, 2017 · Data as of Sep 19, 6:52 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.