GE Inspection Technologies, LP: Medical Device Recall in 2015 - (Recall #: Z-1211-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system

Product Classification:

Class II

Date Initiated: January 13, 2015

Date Posted: April 1, 2015

Recall Number: Z-1211-2015

Event ID: 70478

Reason for Recall:

It was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tome|x L240 installed had lost adhesion and fall out of position, which could lead to gaps in shielding.

Status: Terminated

Product Quantity: 2

Code Information:

SN - PA1260

Distribution Pattern:

US Distribution to the states of OH and PA.

Voluntary or Mandated:

Voluntary: Firm initiated