Has GE Medical Systems, LLC had other FDA enforcement actions?

Yes. Argus HQ has recorded 18 total FDA actions tied to GE Medical Systems, LLC: 0 warning letters, 18 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 2026-06-17; Argus observed and indexed it on 2026-07-09.

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, LLC — Class II recall: Allia IGS Pulse angiographic X-ray system

Name: FDA Recall Record — GE Medical Systems, LLC
Creator: Argus HQ
Published: 2026-06-17
License: https://argushq.ai/methodology

Event date: 2026-06-17 00:00:00Z
Observed: 2026-07-09 22:52:13Z
Source ID: Z-2317-2026
Payload hash: 2711ca73f54606e479a07b8d…

Summary

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabine… Status: Ongoing.

Entities

GE Medical Systems, LLC

View source record ↗

Frequently asked questions

Has GE Medical Systems, LLC had other FDA enforcement actions?: Yes. Argus HQ has recorded 18 total FDA actions tied to GE Medical Systems, LLC: 0 warning letters, 18 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 2026-06-17; Argus observed and indexed it on 2026-07-09.
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, LLC — Class II recall: Allia IGS Pulse angiographic X-ray system. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-ge-medical-systems-llc-z-2317-2026

MLA

"GE Medical Systems, LLC — Class II recall: Allia IGS Pulse angiographic X-ray system." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-ge-medical-systems-llc-z-2317-2026.

Chicago

Argus HQ Research. "GE Medical Systems, LLC — Class II recall: Allia IGS Pulse angiographic X-ray system." Digital Empire Holdings LLC. Accessed August 27, 2026. https://argushq.ai/events/fda-recall-ge-medical-systems-llc-z-2317-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_ge_medical_systems_llc_z_2317_2026_2026,
  title = {GE Medical Systems, LLC — Class II recall: Allia IGS Pulse angiographic X-ray system},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-ge-medical-systems-llc-z-2317-2026},
  note = {Accessed: August 27, 2026}
}

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