How many FDA actions does Argus HQ track for GE Medical Systems Information Technologies Inc?

7 total: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.

What is the most recent FDA action on file for GE Medical Systems Information Technologies Inc?

June 10, 2026. Argus HQ ingests new FDA enforcement records daily.

Has GE Medical Systems Information Technologies Inc had product recalls?

Yes, 7 recalls on file. See the full history below for each one.

Is this FDA enforcement data for GE Medical Systems Information Technologies Inc 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.

GE Medical Systems Information Technologies Inc's Complete FDA Record

FDA action counts

Total FDA actions	7
Warning letters	0
Recalls	7
Approval records	0
Form 483 inspection citations	0
Most recent action	June 10, 2026

The short version: Argus HQ has recorded 7 FDA events for GE Medical Systems Information Technologies Inc: 0 warning letters, 7 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-06-03 to 2026-06-10. 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.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. GE Medical Systems Information Technologies Inc has 7 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.

Enforcement history

On 2026-06-03, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-03, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-03, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; u… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-03, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-03, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orde… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-03, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Pro… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for GE Medical Systems Information Technologies Inc, rated "high" severity in Argus HQ's classification: GE Medical Systems Information Technologies Inc — Class II recall: CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3 An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. In total, GE Medical Systems Information Technologies Inc has 7 FDA events on file with Argus HQ across the sources Argus HQ currently tracks (FDA Warning Letters, recalls, drug/biologic approvals, and Form 483 inspection observations).

Frequently asked questions

How many FDA actions does Argus HQ track for GE Medical Systems Information Technologies Inc?: 7 total: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.
What is the most recent FDA action on file for GE Medical Systems Information Technologies Inc?: June 10, 2026. Argus HQ ingests new FDA enforcement records daily.
Has GE Medical Systems Information Technologies Inc had product recalls?: Yes, 7 recalls on file. See the full history below for each one.
Is this FDA enforcement data for GE Medical Systems Information Technologies Inc 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.

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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's Complete FDA Record. Digital Empire LLC. Retrieved from https://argushq.ai/company/ge-medical-systems-information-technologies-inc

MLA

"GE Medical Systems Information Technologies Inc's Complete FDA Record." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/ge-medical-systems-information-technologies-inc.

Chicago

Argus HQ Research. "GE Medical Systems Information Technologies Inc's Complete FDA Record." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/ge-medical-systems-information-technologies-inc.

BibTeX

@misc{argushq_argushq_ai_company_ge_medical_systems_information_technologies_inc_2026,
  title = {GE Medical Systems Information Technologies Inc's Complete FDA Record},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/ge-medical-systems-information-technologies-inc},
  note = {Accessed: July 13, 2026}
}

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