FDA-Device2025-01-29Class II
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Hazard
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Sold states
Worldwide - US Nationwide distribution.
Affected count
440 units
Manufactured in
7611 Northland Dr N, Brooklyn Park, MN, United States
Products
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0986-2025More Medtronic Perfusion Systems recalls
- FDA-Device2026-05-27Medtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
- FDA-Device2026-05-27Medtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
- FDA-Device2026-05-27Medtronic DLP Retrograde Cannula recalled for potential sterile barrier breach
- FDA-Device2026-05-27Medtronic GUNDRY Retrograde Cannula recalled for sterile barrier breach risk
- FDA-Device2026-05-27Medtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
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