GE Inspection Technologies, LP: Medical Device Recall in 2016 - (Recall #: Z-2236-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis.

Product Classification:

Class II

Date Initiated: March 2, 2016

Date Posted: August 3, 2016

Recall Number: Z-2236-2016

Event ID: 74554

Reason for Recall:

Radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system. The identified cause was insufficient attachment of shielding in the door. Jostling during delivery was identified as the probable cause of this failure to comply with the performance standard.

Status: Terminated

Product Quantity: 4

Code Information:

SN - PA2384

Distribution Pattern:

US Distribution to the states of : FL, TN, and TX.

Voluntary or Mandated:

FDA Mandated