The Recall Desk

Manufacturer

GE Healthcare

89 recalls in our database name GE Healthcare as the manufacturing or recalling firm.

What the numbers show

Total
89
Critical
1
Severe
2
Most recent
2026-03-11

Of the 89 recalls from GE Healthcare we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (2%) 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.

51–75 of 89

  • HighFDA (Devices)·Z-1984-2015·2015-07-08

    GE Healthcare Recalls Innova IGS 630 Angiographic X-ray Systems

    GE Healthcare is recalling eight Innova IGS 630 angiographic X-ray systems due to a potential safety issue that may cause the loss of C-arm gantry motion capability.

    Product
    GE Healthcare Innova IGS 630. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1977-2015·2015-07-08

    GE Healthcare Recalls Innova 2121IQ Angiographic X-ray Systems

    GE Healthcare is recalling Innova 2121IQ angiographic X-ray systems due to a potential loss of C-arm gantry motion capability.

    Product
    GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2015·2015-07-08

    GE Healthcare Recalls Optima CL 323i Angiographic X-ray Systems

    GE Healthcare is recalling seven Optima CL 323i angiographic X-ray systems due to a potential loss of C-arm gantry motion capability.

    Product
    GE Healthcare Optima CL 323i. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1979-2015·2015-07-08

    GE Healthcare Recalls Innova 3131IQ Angiographic X-ray Systems

    GE Healthcare is recalling two Innova 3131IQ angiographic X-ray systems due to a potential safety issue that may result in the loss of C-arm gantry motion capability.

    Product
    GE Healthcare Innova 3131IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1966-2015·2015-07-08

    GE Healthcare Radiographic Systems Recalled for Safety Mechanism Failure

    GE Healthcare is recalling Precision 500D and Advantx Legacy systems because a safety mechanism may fail to engage, posing a risk of injury from falling equipment.

    Product
    GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A universal diagnostic imaging system for radiographic and fluoroscopic examinations. Applications can be performed with the patient sitting, standing, or lying in the prone or sup
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1974-2015·2015-07-08

    GE Healthcare Recalls Discovery IGS 730 Systems Due to Gantry Motion Loss

    GE Healthcare is recalling four Discovery IGS 730 angiographic X-ray systems worldwide due to a potential safety issue that may result in the loss of C-arm gantry motion capability.

    Product
    GE Healthcare Discovery IGS 730. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1825-2015·2015-07-01

    GE Healthcare T2100 Treadmill Recalled for Uncontrolled Walking Belt Motion

    GE Healthcare is recalling 11,423 T2100 Treadmills due to a potential safety issue involving uncontrolled motion of the walking belt.

    Product
    GE Healthcare, Treadmill T2100. For Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1680-2015·2015-06-03

    GE Healthcare Recalls D-Fend Water Traps Due to Occlusion Risk

    GE Healthcare is recalling D-Fend and D-Fend+ water traps because they may occlude, causing a loss of respiratory gas monitoring.

    Product
    D-fend, (p/n 876446-HEL), and D-fend+ (p/n 881319-HEL) water trap. Used with Compact Airway Modules E/M-C(Ai)O(V)(X) and Cardiocap/5 monitors. Product Usage: Water traps are intended to protect the GE monitor from humidity, secretions and bacterial contamination when monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1623-2015·2015-05-27

    GE Healthcare Recalls CT Scanners Due to Over-Torqued Bolts

    GE Healthcare is recalling four CT scanners because over-torqued bolts could cause a component to detach, posing a risk of serious bodily injury.

    Product
    CT LightSpeed 16 and Discovery ST Pet/CT DST. Catalogue # 2339985. Designed to be a head and whole body CT scanner utilizing a new solid state detector.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1606-2015·2015-05-20

    GE Healthcare Recalls CARESCAPE Bx50 Monitors for Pacemaker Detection Defect

    GE Healthcare is recalling 110 CARESCAPE Bx50 monitors because they may fail to indicate when pacemaker detection is off, potentially delaying treatment for asystole.

    Product
    GE Healthcare, CARESCAPE Monitor B850, B650 and B450 (Bx50).
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1405-2015·2015-05-06

    GE Healthcare Recalls Brivo XR285amx Mobile X-Ray Units

    GE Healthcare is recalling six Brivo XR285amx mobile X-ray units in the US due to potential inaccuracies in mAs accuracy checks.

    Product
    GE Healthcare Automatic Mobile X-Ray (AMX) Series: Brivo XR285amx
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1406-2015·2015-05-06

    GE Healthcare Recalls Optima XR200 amx Mobile X-Ray Units

    GE Healthcare is recalling six Optima XR200 amx mobile X-ray units in the US due to potential mAs accuracy issues that may affect exposure times.

    Product
    GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR200 amx
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1407-2015·2015-05-06

    GE Healthcare Recalls Six Optima XR220 amx Mobile X-Ray Units

    GE Healthcare is recalling six Optima XR220 amx mobile X-ray units in the US due to potential mAs accuracy inaccuracies.

    Product
    GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR220 amx
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1441-2015·2015-04-22

    GE Healthcare Recalls Improperly Installed Ceiling Suspended Radiation Shields

    GE Healthcare is recalling 797 ceiling-suspended pendent systems for radiation shields and surgical lamps due to improper installation. One incident of a shield falling and causing a minor injury has been reported.

    Product
    Kenex Radiation Shield installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1376-2015·2015-04-08

    GE Healthcare Recalls Aespire Anesthesia Machines Due to Circuit Board Failure

    GE Healthcare is recalling 46 Aespire 7900 and Aespire View anesthesia machines because a CPU circuit board defect may cause a blank display or loss of mechanical ventilation.

    Product
    GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1305-2015·2015-04-01

    GE Healthcare Recalls MRI Systems Due to Software Maintenance Issues

    GE Healthcare is recalling 9,369 MRI systems worldwide because software versions were not maintained properly at some sites.

    Product
    GE Healthcare, SIGNA 1.5T TWINSPEED, SIGNA INFINITY MRISYSTEM, SIGNA 3.0T INFINITY WITH EXCITE, SIGNA 3.0T WITH EXCITE, SIGNA EXCITE 1.5T, SIGNA EXCITE 3.0T, GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM, Discovery MR750 3.0T, Discovery MR450 1.5T, Discovery MR750w 3.0T, Optima MR450w 1.5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1279-2015·2015-03-25

    GE Healthcare Recalls Nuclear Medicine Systems Due to Collimator Detachment Risk

    GE Healthcare is recalling 472 nuclear medicine systems worldwide because a collimator may fall off during rotation. No injuries have been reported.

    Product
    GE Healthcare Millennium VG, Discovery VH and VariCam Nuclear Medicine systems, all configurations. Product Usage: The intended use of the system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1285-2015·2015-03-25

    GE Healthcare Treadmill T2100 and T2000 Power Cord Recall

    GE Healthcare is recalling T2100 and T2000 treadmills due to a potential safety issue with the power cord assembly.

    Product
    GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field Replaceable Unit P/Ns 408930-001 Rev E, 408930-002 Rev C. UPDATE: 3-30-2015: T2100 & T2000 Treadmills with power cord part
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1270-2015·2015-03-25

    GE Healthcare Ventilators Recalled for Caster Mounting Hardware Failure Risk

    GE Healthcare is recalling specific ventilator models due to a potential failure of the caster mounting hardware that could cause the device to fall or tip over.

    Product
    GE Healthcare Engstrom Carestation, Engstrom Pro, Cart Only S/5 EC. GE model numbers 1505-8538-000, 1505-9000-000, and 1505-9003-000. Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1248-2015·2015-03-18

    GE Healthcare Recalls Proteus XR/a X-ray Systems Due to Cable Breakage Risk

    GE Healthcare is recalling Proteus XR/a X-ray systems because a steel cable supporting the bucky device may break. A falling bucky could injure a patient or operator.

    Product
    GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of human anatomy in all general purpose diagnostic procedures. This device is not intended for mammographic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1214-2015·2015-03-04

    GE Healthcare Recalls Centricity PACS Workstation Due to Exam Merge Failure

    GE Healthcare is recalling 128 Centricity PACS Workstation systems because a software defect may cause exam records to go missing in single Study Mode.

    Product
    The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professionals, including radiologists, physicians, technologists, clinicians and nurses. It is also intended for use as a clinical review work
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1035-2015·2015-02-25

    GE Healthcare MRI Systems Recalled for Potential Ferrous Object Removal Delay

    GE Healthcare is recalling MRI systems because a disconnected MRU could delay the removal of ferrous objects, posing a life-threatening injury risk.

    Product
    This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, GE 1.5T Signa HDe, Optima MR360, Brivo MR355, Signa Excite-HD 1.5T & 3T, Signa Excite 1.5T HD Twinspeed, Signa Excite 1.5T HD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0955-2015·2015-02-04

    GE Healthcare Recalls Revolution CT Scanners Due to Missing Quality Control Test

    GE Healthcare is recalling 13 Revolution CT scanners because a required quality control test was not performed during installation.

    Product
    The Revolution CT is a multi-slice (256 detector row) CT scanner consisting of a gantry, patient table, scanner desktop (operator console), system cabinet, power distribution unit (POU). and interconnecting cables.The system includes image acquisition hardware, image acquisition
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0966-2015·2015-01-21

    GE Healthcare Recalls Discovery IGS 730 and 740 X-ray Systems

    GE Healthcare is recalling 24 Discovery IGS 730 and 740 angiographic X-ray systems due to a user interface issue that may cause unintentional system motion or rotation.

    Product
    GE Healthcare, Discovery IGS 730 & Discovery IGS 740. Discovery IGS 730 : The angiographic X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular & non vascular diagnostic and interventional procedures
    Category
    Medical Device
    Distribution
    7 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

GE HealthCare

American multinational medical technology company

Country
United States
Founded
2004

Official website

Source: Wikidata (Q1152374), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.