Skip to main content

fda_recall · device_recall · high

Medtronic Perfusion Systems — Class II recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014…

Event date
2025-01-29 00:00:00Z
Observed
2026-07-16 23:20:07Z
Source ID
Z-0984-2025
Payload hash
88a9b24daef132286c14302f…

Summary

Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae. Status: Ongoing.

Entities

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 high severity by Argus HQ. FDA published the underlying record on 2025-01-29; 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 II recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-0984-2025
MLA
"Medtronic Perfusion Systems — Class II recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-0984-2025.
Chicago
Argus HQ Research. "Medtronic Perfusion Systems — Class II recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-0984-2025.
BibTeX
@misc{argushq_argushq_ai_events_fda_recall_medtronic_perfusion_systems_z_0984_2025_2025,
  title = {Medtronic Perfusion Systems — Class II recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-perfusion-systems-z-0984-2025},
  note = {Accessed: July 23, 2026}
}

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

Medtronic Perfusion Systems — Class II recall: DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014… · Argus HQ