GE Inspection Technologies Blade|line Industrial recall
GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Why was GE Inspection Technologies Blade|line Industrial 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
- Recalling firm
- GE Inspection Technologies, LP
- Quantity
- 13 units distributed in the US
- Distribution
- US Distribution to the states of : AL, SC, OH, MI, PA, and Internationally to Germany and Singapore
- Recall date
- August 9, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)