The Recall Desk

Manufacturer

GE Inspection Technologies, LP

7 recalls in our database name GE Inspection Technologies, LP as the manufacturing or recalling firm.

What the numbers show

Total
7
Critical
0
Severe
1
Most recent
2017-08-09

Of the 7 recalls from GE Inspection Technologies, LP we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (14%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–7 of 7

  • ModerateFDA (Devices)·Z-2777-2017·2017-08-09

    GE Blade|line Industrial Cabinet X-ray System Recalled for Emission Violations

    GE Inspection Technologies is recalling 13 Blade|line Industrial Cabinet X-ray systems because they exceed federal emission limits in an inaccessible crawl space.

    Product
    GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
    Category
    Medical Device
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2236-2016·2016-08-03

    GE Phoenix v|tome|x m240 X-Ray Systems Recalled for Radiation Emissions

    GE Inspection Technologies is recalling four Phoenix v|tome|x m240 cabinet x-ray systems because radiation emissions exceeded safety limits due to insufficient door shielding.

    Product
    GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1231-2016·2016-04-13

    GE Cabinet X-ray Systems Recalled for Non-Compliance with FDA Standards

    GE Inspection Technologies is recalling 55 cabinet x-ray systems used for industrial quality control because they may not fully comply with FDA performance standards.

    Product
    GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
    Category
    Medical Device
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-2320-2015·2015-08-19

    GE Laser Centering Device Recalled for Regulatory Non-Compliance

    GE Inspection Technologies is recalling 25 laser centering devices for X-ray generators due to potential failure to comply with federal regulations.

    Product
    GE Optional Laser Centering Device X-ray generator.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-1211-2015·2015-04-01

    GE x|tome|x L240 X-ray System Recalled for Lead Shield Defect

    GE Inspection Technologies is recalling two x|tome|x L240 X-ray systems because a lead shield fell out of position, creating potential radiation exposure gaps.

    Product
    GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1225-2015·2015-04-01

    GE x|argos 160D Cabinet X-Ray System Recalled for Shielding Defect

    GE Inspection Technologies is recalling two x|argos 160D cabinet x-ray systems because a lead shield fell out of position, creating potential radiation gaps.

    Product
    GE Inspection Technologies x|argos 160D system. Cabinet x-ray system.
    Category
    Medical Device
    Distribution
    2 states