Select Series® 72520Recalls & reported problems

Medtronic, Inc. · CANNULA 72520 SELECT ART 45 20F 20P 17L · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20613994879749), received between Apr 22, 2024 and Apr 22, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K840002); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Fluid/Blood Leak1
Material Puncture/Hole1

Patient problems

Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryApr 22, 2024Fluid/Blood Leak; Material Puncture/Hole; Fluid/Blood Leak; Material Puncture/Hole
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A SELECT SERIES ANGLED TIP ARTERIAL CANNULA, IT WAS REPORTED THAT WHEN INSERTING THE DEVICE FOR CIRCULATION EXTRA-CORPORELLE (CEC), A LEAK WAS OBSERVED ON THE DISTAL END OF THE CANNULA. THE CUSTOMER ALSO OBSERVED A HOLE SEVERAL MILLIMETRES IN SIZE. THE CUSTOMER STATED THE CEC CIRCUIT WAS UNSEALED. THERE WAS PATIENT BLOOD LOSS AS A RESULT OF THE LEAK. THE USE OF THE DEVICE WAS UNSPECIFIED. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19150789 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K840002. One submission often covers many models, so check the product and lot details in each record.

Z-0986-2025 · Dec 12, 2024 · Open, Classified
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Z-1793-2024 · Mar 19, 2024 · Open, Classified
Medtronic Arterial Cannulae packaged as: a) DLP Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020; b) DLP Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220
Z-1927-2008 · May 9, 2008 · Terminated
Medtronic Arterial Cannula Curved Beveled Tip, for Cardiopulmonary Bypass. Catalog Numbers: CB81120 and CB87022.

Device details

UDI-DI	`20613994879749`
Brand	Select Series®
Model	72520
Company	Medtronic, Inc.
Product code	DWF · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
Class	Class 2
FDA submission	K840002
Implant	No
Rx / OTC	—
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 19, 2024

Device type (GMDN): Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return

A semi-rigid or rigid tube intended to be surgically inserted into an artery or vein to serve as a channel for the extracorporeal transport of oxygenated blood to a patient during cardiopulmonary bypass and/or extracorporeal membrane oxygenation; in some settings it may be referred to as an arterial cannula. It is typically inserted using a compatible trocar blade which may be included. This is a single-use device.

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All CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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