How many FDA warning letters has GE Healthcare Ireland Limited received?

Argus HQ has not recorded an FDA warning letter for GE Healthcare Ireland Limited in our current dataset.

What FDA recalls has GE Healthcare Ireland Limited issued?

Argus HQ has recorded 2 FDA recalls tied to GE Healthcare Ireland Limited.

Is GE Healthcare Ireland Limited FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for GE Healthcare Ireland Limited. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

GE Healthcare Ireland Limited

Name: FDA Enforcement Actions Against GE Healthcare Ireland Limited
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 · drug_recall2026-04-15
GE Healthcare Ireland Limited — Class II recall: GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distrib…
fda_recall · drug_recall2026-04-15
GE Healthcare Ireland Limited — Class II recall: GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distrib…

Frequently asked questions

How many FDA warning letters has GE Healthcare Ireland Limited received?: Argus HQ has not recorded an FDA warning letter for GE Healthcare Ireland Limited in our current dataset.
What FDA recalls has GE Healthcare Ireland Limited issued?: Argus HQ has recorded 2 FDA recalls tied to GE Healthcare Ireland Limited.
Is GE Healthcare Ireland Limited FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for GE Healthcare Ireland Limited. 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.