Is this FDA enforcement data for GE Healthcare official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

How many FDA actions has GE Healthcare had?

Argus HQ has recorded 18 FDA events for GE Healthcare: 0 warning letters, 18 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

What is the most recent FDA action against GE Healthcare?

The most recent FDA event Argus HQ has on file for GE Healthcare is dated 2026-03-11, with a severity rating of "high" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Does Argus HQ track new FDA actions for GE Healthcare automatically?

Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to GE Healthcare is observed, this page's event count and history update automatically.

Regulatory Record: GE Healthcare

FDA action counts

Total FDA actions	18
Warning letters	0
Recalls	18
Approval records	0
Form 483 inspection citations	0
Most recent action	March 11, 2026

The short version: Argus HQ has recorded 18 FDA events for GE Healthcare: 0 warning letters, 18 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2023-05-10 to 2026-03-11. The most severe rating Argus HQ has assigned across this history is "high". Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Enforcement history

On 2026-03-11, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers:…. On 2025-04-09, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers: 1) 2022296-0…. On 2025-04-09, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers…. On 2025-04-09, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Universal Viewer (UV), Model Numbers: 1) 2066908-077;…. On 2025-04-09, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Cardiology CA1000 (CA1000), Model Numbers: 1) 203390…. On 2025-04-09, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity PACS-IW (PACS-IW), Model Numbers: 1) 2042988-001;…. On 2024-11-13, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2…. On 2024-10-16, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/C…. On 2024-10-02, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricty PACS, V2, V3, V4, V6, V7; Radiological imaging processin…. On 2024-09-25, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers:…. On 2023-11-01, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: Centricity PACS-IW, software versions V3.7.x through 3.7.3.9 SP3; Radiological I…. On 2023-11-01, Argus HQ recorded an FDA recall for GE Healthcare, rated "high" severity in Argus HQ's classification: GE Healthcare — Class II recall: Universal Viewer Workflow Manager, Image processing radiological system.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. GE Healthcare has 18 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Frequently asked questions

Is this FDA enforcement data for GE Healthcare official?: Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
How many FDA actions has GE Healthcare had?: Argus HQ has recorded 18 FDA events for GE Healthcare: 0 warning letters, 18 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
What is the most recent FDA action against GE Healthcare?: The most recent FDA event Argus HQ has on file for GE Healthcare is dated 2026-03-11, with a severity rating of "high" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
Does Argus HQ track new FDA actions for GE Healthcare automatically?: Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to GE Healthcare is observed, this page's event count and history update automatically.

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

Verified from FDA.gov · Last updated: Mar 11, 2026

Cite this record

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

APA

Argus HQ Research (2026). Regulatory Record: GE Healthcare. Digital Empire LLC. Retrieved from https://argushq.ai/company/ge-healthcare

MLA

"Regulatory Record: GE Healthcare." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/ge-healthcare.

Chicago

Argus HQ Research. "Regulatory Record: GE Healthcare." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/company/ge-healthcare.

BibTeX

@misc{argushq_argushq_ai_company_ge_healthcare_2026,
  title = {Regulatory Record: GE Healthcare},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/ge-healthcare},
  note = {Accessed: July 17, 2026}
}

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗