Select Series® 72420Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 20643169485963), received between May 24, 2023 and Nov 25, 2024 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (3 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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 25, 2024Material Deformation; Material Deformation

  MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A SELECT SERIES ANGLED TIP ARTERIAL CANNULA, IT WAS REPORTED THAT THE PACKAGE WAS OPENED AND IT WAS FOUND THAT THE BLUE CAP AT THE END OF THE CANNULA WAS DAMAGED. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20770007 ↗
• MalfunctionMay 24, 2023Material Deformation; Material Deformation

  MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A 72420 SELECT SERIES ANGLED TIP ARTERIAL CANNULA, THE CUSTOMER REPORTED THAT THE CANNULA WAS BENT/KINKED. IT WAS ASKED BUT UNKNOWN WHETHER THE DEVICE WAS REPLACED. THE CANNULA WAS NOT USED. THERE WAS NO PATIENT INVOLVEMENT SO NO ADVERSE EFFECT OCCURRED. ADDITIONAL INFORMATION: THE KINK WAS NOTED BEFORE UNPACKING THE CANNULA. THERE WAS NO ATTEMPT MADE TO USE THE CANNULA.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16992285 ↗
• MalfunctionMay 24, 2023Material Deformation; Material Deformation

  MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE, THE CUSTOMER REPORTED THE ANGLED TIP ARTERIAL CANNULA WAS DEFORMED/INDENTED. THE DEVICE WILL BE REPLACED IN THE FUTURE. THERE WAS NO PATIENT INVOLVEMENT SO NO ADVERSE EFFECT OCCURRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16992084 ↗

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.