How many FDA warning letters has Medtronic, Inc. received?

Argus HQ has not recorded an FDA warning letter for Medtronic, Inc. in our current dataset.

What FDA recalls has Medtronic, Inc. issued?

Argus HQ has recorded 1 FDA recall tied to Medtronic, Inc..

Is Medtronic, Inc. 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 Medtronic, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Medtronic, Inc.

Name: FDA Enforcement Actions Against Medtronic, Inc.
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_recall2026-05-06
Medtronic, Inc. — Class II recall: Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, car…

Frequently asked questions

How many FDA warning letters has Medtronic, Inc. received?: Argus HQ has not recorded an FDA warning letter for Medtronic, Inc. in our current dataset.
What FDA recalls has Medtronic, Inc. issued?: Argus HQ has recorded 1 FDA recall tied to Medtronic, Inc..
Is Medtronic, Inc. 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 Medtronic, Inc.. 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.