How many FDA warning letters has GE Medical Systems, LLC received?

Argus HQ has not recorded an FDA warning letter for GE Medical Systems, LLC in our current dataset.

What FDA recalls has GE Medical Systems, LLC issued?

Argus HQ has recorded 15 FDA recalls tied to GE Medical Systems, LLC.

Is GE Medical Systems, LLC FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 15 recalls, and 0 approval records for GE Medical Systems, LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

GE Medical Systems, LLC

Name: FDA Enforcement Actions Against GE Medical Systems, LLC
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-06-24
GE Medical Systems, LLC — Class II recall: Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 66…
fda_recall · device_recall2026-06-24
GE Medical Systems, LLC — Class II recall: Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination…
fda_recall · device_recall2026-06-24
GE Medical Systems, LLC — Class II recall: Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All…
fda_recall · device_recall2026-06-17
GE Medical Systems, LLC — Class II recall: Allia IGS 3 Pulse angiographic X-ray system
fda_recall · device_recall2026-06-17
GE Medical Systems, LLC — Class II recall: Allia IGS 7 Pulse angiographic X-ray system
fda_recall · device_recall2026-06-17
GE Medical Systems, LLC — Class II recall: Allia IGS 5 Pulse angiographic X-ray system
fda_recall · device_recall2026-06-17
GE Medical Systems, LLC — Class II recall: Allia Moveo angiographic X-ray system
fda_recall · device_recall2026-06-17
GE Medical Systems, LLC — Class II recall: Allia IGS Pulse angiographic X-ray system
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25
fda_recall · device_recall2026-05-20
GE Medical Systems, LLC — Class II recall: Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-30…

Frequently asked questions

How many FDA warning letters has GE Medical Systems, LLC received?: Argus HQ has not recorded an FDA warning letter for GE Medical Systems, LLC in our current dataset.
What FDA recalls has GE Medical Systems, LLC issued?: Argus HQ has recorded 15 FDA recalls tied to GE Medical Systems, LLC.
Is GE Medical Systems, LLC FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 15 recalls, and 0 approval records for GE Medical Systems, LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.