The Recall Desk

Manufacturer

GE Vingmed Ultrasound As

6 recalls in our database name GE Vingmed Ultrasound As as the manufacturing or recalling firm.

What the numbers show

Total
6
Critical
0
Severe
0
Most recent
2024-07-17

Of the 6 recalls from GE Vingmed Ultrasound As we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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.

1–6 of 6

  • HighFDA (Devices)·Z-2317-2024·2024-07-17

    GE Vivid Ultrasound Scanner Displays Incorrect Patient Data

    GE Vivid ultrasound systems may display incorrect patient names and demographics due to slow DICOM response times, risking patient misidentification during imaging.

    Product
    GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-2316-2024·2024-07-17

    GE Vivid Ultrasound Systems Display Incorrect Patient Names

    GE Vivid ultrasound systems may display incorrect patient information due to slow DICOM response times. Seven affected units were distributed to healthcare facilities in IL, MA, NM, NY, and OK.

    Product
    GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-2126-2023·2023-07-19

    GE Healthcare Vivid S60N ultrasound devices experience boot-up delays

    GE Healthcare Vivid S60N ultrasound systems may fail to boot in a timely manner. This can delay device availability during time-critical emergency situations.

    Product
    GE Healthcare Vivid S60N, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2124-2023·2023-07-19

    Ultrasound Device Boot Failure May Delay Emergency Availability

    Certain GE HealthCare Vivid S60 ultrasound systems may not boot up in a timely fashion, potentially delaying device availability in time-critical emergency situations.

    Product
    GE Healthcare Vivid S60, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2125-2023·2023-07-19

    GE Healthcare Vivid S70 ultrasound systems fail to boot timely

    GE Healthcare Vivid S70 ultrasound devices may experience delayed startup. This can reduce equipment availability during time-critical emergency situations.

    Product
    GE Healthcare Vivid S70, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2127-2023·2023-07-19

    GE Vivid S70N Ultrasound Device Boot Failure Recall

    GE Healthcare recalls certain Vivid S70N ultrasound devices that may not boot promptly, potentially delaying availability in time-critical emergencies.

    Product
    GE Healthcare Vivid S70N, ultrasound device
    Category
    Medical Device
    Distribution
    0 states