Has GE Healthcare (China) Co., Ltd. had other FDA enforcement actions?

Yes. Argus HQ has recorded 24 total FDA actions tied to GE Healthcare (China) Co., Ltd.: 0 warning letters, 24 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 2024-09-04; Argus observed and indexed it on 2026-07-16.

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 Healthcare (China) Co., Ltd. — Class II recall: GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers: 1…

Name: FDA Recall Record — GE Healthcare (China) Co., Ltd.
Creator: Argus HQ
Published: 2024-09-04
License: https://argushq.ai/methodology

Event date: 2024-09-04 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-2733-2024
Payload hash: 00efcd934c4637221c31ca95…

Summary

The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to avoid personnel injury during de-install. Status: Ongoing.

Entities

GE Healthcare (China) Co., Ltd.

View source record ↗

Frequently asked questions

Has GE Healthcare (China) Co., Ltd. had other FDA enforcement actions?: Yes. Argus HQ has recorded 24 total FDA actions tied to GE Healthcare (China) Co., Ltd.: 0 warning letters, 24 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 2024-09-04; Argus observed and indexed it on 2026-07-16.
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 (2024). GE Healthcare (China) Co., Ltd. — Class II recall: GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers:    1…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-ge-healthcare-china-co-ltd-z-2733-2024

MLA

"GE Healthcare (China) Co., Ltd. — Class II recall: GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers:    1…." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-ge-healthcare-china-co-ltd-z-2733-2024.

Chicago

Argus HQ Research. "GE Healthcare (China) Co., Ltd. — Class II recall: GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers:    1…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-ge-healthcare-china-co-ltd-z-2733-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_ge_healthcare_china_co_ltd_z_2733_2024_2024,
  title = {GE Healthcare (China) Co., Ltd. — Class II recall: GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers:    1…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-ge-healthcare-china-co-ltd-z-2733-2024},
  note = {Accessed: July 17, 2026}
}

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