Reported Aug 9, 2017 · Terminated

GE Inspection Technologies Blade|line Industrial Cabinet X-ray system

GE Inspection Technologies, LP

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: GE Inspection Technologies, LP · 50 Industrial Park Rd · Lewistown, PA · 17044-9312

Is this the product you have?

  • GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Lot codes and dates
  • Serial No. TM 201317 TM 201312 TM 201323 TM 201331 TM 201401 TM 201329 TM 201404 TM 201413 TM 201414 TM 201415 TM 201424 TM 201425 158017R1
Amount recalled
13 units distributed in the US

Where it was sold

Why it was recalled

GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the cabinet x-ray performance standards emission limit of 0.5 milliRoentgen in one hour (21 CFR ¿ 1020.40(c)(1)(i)) underneath the bottom center of the system. The crawl space affected by the excess emission is approximately 22 inches high, normally covered by decorative panels, and is not intended to be accessed.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 6, 2020 · Data as of Sep 19, 6:06 PM UTC

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