DLP® 88024Recalls & reported problems

Medtronic, Inc. · CANNULA 88024 ART CUR TIP 24FR 20PK 17L · Class 2

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20643169485642), received between Nov 20, 2023 and Nov 20, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

Component Missing1
Fluid/Blood Leak1

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.

MalfunctionNov 20, 2023Fluid/Blood Leak; Component Missing; Fluid/Blood Leak; Component Missing
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A DLP CURVED TIP ARTERIAL CANNULA, IT WAS REPORTED THAT UPON CANNULATION IT WAS UN FORTUNATELY NOTED THAT THE WHITE FILTER WAS NOT IN THE CANNULA CAP WHICH CAUSED A BLOOD SURGE OUT THE END OF THE CANNULA. THE DEVICE WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE PATIENT BLOOD LOSS WAS ESTIMATED AT 100ML. THERE WAS NO UNPLANNED TRANSFUSION REQUIRED AS A RESULT OF THIS.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 18169372 ↗

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	`20643169485642`
Brand	DLP®
Model	88024
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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