How many FDA warning letters has Medtronic Perfusion Systems received?

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

What FDA recalls has Medtronic Perfusion Systems issued?

Argus HQ has recorded 12 FDA recalls tied to Medtronic Perfusion Systems.

Is Medtronic Perfusion Systems FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 12 recalls, and 0 approval records for Medtronic Perfusion Systems. Review the linked FDA source records directly before drawing a compliance conclusion.

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Medtronic Perfusion Systems

Name: FDA Enforcement Actions Against Medtronic Perfusion Systems
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_recall2026-07-01
Medtronic Perfusion Systems — Class II recall: Octopus Evolution Tissue Stabilizer, Model TS2000
fda_recall · device_recall2026-07-01
Medtronic Perfusion Systems — Class II recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500
fda_recall · device_recall2026-07-01
Medtronic Perfusion Systems — Class II recall: Octopus 4 Tissue Stabilizer, Model 29400
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 9…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94…
fda_recall · device_recall2026-05-27
Medtronic Perfusion Systems — Class II recall: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94…

Frequently asked questions

How many FDA warning letters has Medtronic Perfusion Systems received?: Argus HQ has not recorded an FDA warning letter for Medtronic Perfusion Systems in our current dataset.
What FDA recalls has Medtronic Perfusion Systems issued?: Argus HQ has recorded 12 FDA recalls tied to Medtronic Perfusion Systems.
Is Medtronic Perfusion Systems FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 12 recalls, and 0 approval records for Medtronic Perfusion Systems. 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.