Has Medtronic Perfusion Systems had other FDA enforcement actions?

Yes. Argus HQ has recorded 46 total FDA actions tied to Medtronic Perfusion Systems: 0 warning letters, 46 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2025-09-10; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · critical

Medtronic Perfusion Systems — Class I recall: DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113…

Name: FDA Recall Record — Medtronic Perfusion Systems
Creator: Argus HQ
Published: 2025-09-10
License: https://argushq.ai/methodology

Event date: 2025-09-10 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: Z-2480-2025
Payload hash: 3e73075590330999f4c3f160…

Summary

The catheters may not retain their shape. Status: Ongoing.

Entities

Medtronic Perfusion Systems

View source record ↗

Frequently asked questions

Has Medtronic Perfusion Systems had other FDA enforcement actions?: Yes. Argus HQ has recorded 46 total FDA actions tied to Medtronic Perfusion Systems: 0 warning letters, 46 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2025-09-10; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2025). Medtronic Perfusion Systems — Class I recall: DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2480-2025

MLA

"Medtronic Perfusion Systems — Class I recall: DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2480-2025.

Chicago

Argus HQ Research. "Medtronic Perfusion Systems — Class I recall: DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2480-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medtronic_perfusion_systems_z_2480_2025_2025,
  title = {Medtronic Perfusion Systems — Class I recall: DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2480-2025},
  note = {Accessed: July 23, 2026}
}

Informational only. Not legal, financial, or medical advice.