Has Medtronic Perfusion Systems had other FDA enforcement actions?

Yes. Argus HQ has recorded 54 total FDA actions tied to Medtronic Perfusion Systems: 0 warning letters, 54 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 high severity by Argus HQ. FDA published the underlying record on 2026-07-01; Argus observed and indexed it on 2026-07-09.

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 · high

Medtronic Perfusion Systems — Class II recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500

Name: FDA Recall Record — Medtronic Perfusion Systems
Creator: Argus HQ
Published: 2026-07-01
License: https://argushq.ai/methodology

Event date: 2026-07-01 00:00:00Z
Observed: 2026-07-09 22:51:53Z
Source ID: Z-2576-2026
Payload hash: 7308072936ead760494be0ff…

Summary

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design. 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 54 total FDA actions tied to Medtronic Perfusion Systems: 0 warning letters, 54 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 high severity by Argus HQ. FDA published the underlying record on 2026-07-01; Argus observed and indexed it on 2026-07-09.
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 (2026). Medtronic Perfusion Systems — Class II recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2576-2026

MLA

"Medtronic Perfusion Systems — Class II recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2576-2026.

Chicago

Argus HQ Research. "Medtronic Perfusion Systems — Class II recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500." Digital Empire Holdings LLC. Accessed August 27, 2026. https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2576-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medtronic_perfusion_systems_z_2576_2026_2026,
  title = {Medtronic Perfusion Systems — Class II recall: Octopus Evolution AS Tissue Stabilizer, Model TS2500},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-2576-2026},
  note = {Accessed: August 27, 2026}
}

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