How many FDA warning letters has GE Medical Systems China Co., Ltd. received?

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

What FDA recalls has GE Medical Systems China Co., Ltd. issued?

Argus HQ has recorded 1 FDA recall tied to GE Medical Systems China Co., Ltd..

Is GE Medical Systems China Co., Ltd. FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for GE Medical Systems China Co., Ltd.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

GE Medical Systems China Co., Ltd.

Name: FDA Enforcement Actions Against GE Medical Systems China Co., Ltd.
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_recall2026-06-10
GE Medical Systems China Co., Ltd. — Class II recall: MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis…

Frequently asked questions

How many FDA warning letters has GE Medical Systems China Co., Ltd. received?: Argus HQ has not recorded an FDA warning letter for GE Medical Systems China Co., Ltd. in our current dataset.
What FDA recalls has GE Medical Systems China Co., Ltd. issued?: Argus HQ has recorded 1 FDA recall tied to GE Medical Systems China Co., Ltd..
Is GE Medical Systems China Co., Ltd. FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for GE Medical Systems China Co., Ltd.. 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.