GE Inspection Technologies, LP: Medical Device Recall in 2017 - (Recall #: Z-2777-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 28, 2017

Date Posted: August 9, 2017

Recall Number: Z-2777-2017

Event ID: 77756

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.

Status: Terminated

Product Quantity: 13 units distributed in the US

Code Information:

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

Distribution Pattern:

US Distribution to the states of : AL, SC, OH, MI, PA, and Internationally to Germany and Singapore

Voluntary or Mandated:

FDA Mandated