Has GE Healthcare Finland Oy had other FDA enforcement actions?

Yes. Argus HQ has recorded 19 total FDA actions tied to GE Healthcare Finland Oy: 0 warning letters, 19 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 2024-07-03; 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 Finland Oy — Class II recall: CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c)…

Name: FDA Recall Record — GE Healthcare Finland Oy
Creator: Argus HQ
Published: 2024-07-03
License: https://argushq.ai/methodology

Event date: 2024-07-03 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-2169-2024
Payload hash: f94f90bf15e008644ba8f12e…

Summary

GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650 monitors if, following the replacement of the CPU timekeeper battery, a mains power loss occurs during active mon… Status: Ongoing.

Entities

GE Healthcare Finland Oy

View source record ↗

Frequently asked questions

Has GE Healthcare Finland Oy had other FDA enforcement actions?: Yes. Argus HQ has recorded 19 total FDA actions tied to GE Healthcare Finland Oy: 0 warning letters, 19 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 2024-07-03; 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 Finland Oy — Class II recall: CARESCAPE Canvas Smart Display, Model Numbers:   a) 5700023,  b) 5700023-02,  c)…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-ge-healthcare-finland-oy-z-2169-2024

MLA

"GE Healthcare Finland Oy — Class II recall: CARESCAPE Canvas Smart Display, Model Numbers:   a) 5700023,  b) 5700023-02,  c)…." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-ge-healthcare-finland-oy-z-2169-2024.

Chicago

Argus HQ Research. "GE Healthcare Finland Oy — Class II recall: CARESCAPE Canvas Smart Display, Model Numbers:   a) 5700023,  b) 5700023-02,  c)…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-ge-healthcare-finland-oy-z-2169-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_ge_healthcare_finland_oy_z_2169_2024_2024,
  title = {GE Healthcare Finland Oy — Class II recall: CARESCAPE Canvas Smart Display, Model Numbers:   a) 5700023,  b) 5700023-02,  c)…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-ge-healthcare-finland-oy-z-2169-2024},
  note = {Accessed: July 17, 2026}
}

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