GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
FDA Recall Z-2777-2017 · Posted None
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Recalling FirmGE Inspection Technologies, LP
Recall StatusTerminated
Product CodeRCE
Date Initiated2017-06-28
Date Terminated2020-02-06
Product Quantity13 units distributed in the US
Reason for Recall
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.
Firm Action
GE Inspection Technologies will bring the defect into compliance:
1. Four panels of sheet metal/lead/sheet metal construction (6 mm lead thickness) will be permanently mounted using an industrial epoxy to the inside floor of the cabinet to prevent emissions from exceeding the limit in the performance standard. A radiation emission measurement will be made following the repairs of each system to assure the issue was corrected.
2. GE will notify affected customers within 5 days of GEs receipt of this approval letter.
3. The notification will recommend that customers allow GE to visit the site and install the new shielding within 120 days following GEs receipt of this letter.
4.The text of the notification to customers will include the required statement that confirms that GE will, without charge, bring the affected cabinet x-ray systems into compliance with the performance standard. For further questions, please call (717) 447-1278.
Root Cause
Radiation Control for Health and Safety Act
Distribution Pattern
US Distribution to the states of : AL, SC, OH, MI, PA, and Internationally to Germany and Singapore
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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