Select Series® 72122Recalls & reported problems
Medtronic, Inc. · CANNULA 72122 SELECT ART STR 22F 20P 17 · Class 2
All models of Select Series (8)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20643169485949), received between May 22, 2023 and Sep 14, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Separation” (2 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Separation2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2026Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50757074 ↗MalfunctionMay 22, 2023Material Separation; Material Separation
MEDTRONIC RECEIVED INFORMATION THAT DURING USE, THE CUSTOMER REPORTED THE 22FR ARTERIAL CANNULA CONNECTOR, NORMALLY GLUED TO THE AORTIC CANNULA, FELL OFF DURING PROCEDURE RIGHT BEFORE CONNECTING TO TUBING SET OF HLM. THE DEVICE WAS REPLACED. THERE WAS NO ADVERSE EFFECT TO THE PATIENT. THE CUSTOMER STATED A DANGEROUS SITUATION OCCURRED. AN UNKNOWN AMOUNT BLOOD LEAKED OUT OF THE CANNULA (IN ADDITION, THEY STATED AIR COULD HAVE ENTERED). IT WAS ASKED BUT UNKNOWN IF A BLOOD TRANSFUSION WAS REQUIRED AS A RESULT OF THE LEAK. SITUATION WAS MANAGED AND PATIENT OKAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16973076 ↗
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 HY11R00R6Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls3 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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