DLP® 88020Recalls & reported problems
Medtronic, Inc. · CANNULA 88020 ART CUR TIP 22FR 20PK 17L · Class 2
- 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 20643169485628), received between Jul 30, 2025 and Jul 30, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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
Most reported problems
Device problems
- Material Deformation1
- Obstruction of Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 30, 2025Obstruction of Flow; Material Deformation; Obstruction of Flow; Material Deformation
IT WAS REPORTED THAT DURING USE OF THE DLP CURVED TIP ARTERIAL CANNULA, A PRESSURE DROP WAS OBSERVED. THE TIP OF THE CANNULA WAS FOUND TO BE KINKED, RESULTING IN ONLY 25% OF THE LUMEN BEING AVAILABLE. THE SURGEON VERIFIED THE POSITION OF THE CANNULA AND THEN DECIDED TO CHANGE IT. UPON REMOVAL; THE KINKED TIP AND REDUCED LUMEN WERE CONFIRMED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22662448 ↗
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, ClassifiedSelect Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
- Z-1793-2024 · Mar 19, 2024 · Open, ClassifiedMedtronic 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 · TerminatedMedtronic Arterial Cannula Curved Beveled Tip, for Cardiopulmonary Bypass. Catalog Numbers: CB81120 and CB87022.
Other CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS devices
- DLP™ 77010Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall154 reports
- EOPA™ 77422Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls19 reports
- DLP™ 77008Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls9 reports
- NA HY11W65R1Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls8 reports
- DLP® 12113Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls6 reports
- DLP® Aortic Root Cannula with Flow-Guard™ 11012Medtronic, Inc. · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 recalls5 reports
- EOPA™ 77622Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls4 reports
- NA HY2V10R33Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls3 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.