Has GE Medical Systems Information Technologies Inc had other FDA enforcement actions?

Yes. Argus HQ has recorded 9 total FDA actions tied to GE Medical Systems Information Technologies Inc: 0 warning letters, 9 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-08-12; Argus observed and indexed it on 2026-08-19.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

GE Medical Systems Information Technologies Inc — Class II recall: GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph

Name: FDA Recall Record — GE Medical Systems Information Technologies Inc
Creator: Argus HQ
Published: 2026-08-12
License: https://argushq.ai/methodology

Event date: 2026-08-12 00:00:00Z
Observed: 2026-08-19 04:20:39Z
Source ID: Z-2876-2026
Payload hash: 4559d4bca4c33ad5994cd593…

Summary

Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity. As a result, data from a previous patient may remain on the screen and could be incorrectly associated with… Status: Ongoing.

Entities

GE Medical Systems Information Technologies Inc

View source record ↗

Frequently asked questions

Has GE Medical Systems Information Technologies Inc had other FDA enforcement actions?: Yes. Argus HQ has recorded 9 total FDA actions tied to GE Medical Systems Information Technologies Inc: 0 warning letters, 9 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-08-12; Argus observed and indexed it on 2026-08-19.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). GE Medical Systems Information Technologies Inc — Class II recall: GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-ge-medical-systems-information-technologies-inc-z-2876-2026

MLA

"GE Medical Systems Information Technologies Inc — Class II recall: GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-ge-medical-systems-information-technologies-inc-z-2876-2026.

Chicago

Argus HQ Research. "GE Medical Systems Information Technologies Inc — Class II recall: GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph." Digital Empire Holdings LLC. Accessed August 19, 2026. https://argushq.ai/events/fda-recall-ge-medical-systems-information-technologies-inc-z-2876-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_ge_medical_systems_information_technologies_inc_z_2876_2026_2026,
  title = {GE Medical Systems Information Technologies Inc — Class II recall: GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-ge-medical-systems-information-technologies-inc-z-2876-2026},
  note = {Accessed: August 19, 2026}
}

Informational only. Not legal, financial, or medical advice.