FDA-Device2024-05-22Class II
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Hazard
Potential for unsealed sterile packing.
Sold states
Worldwide distribution.
Affected count
250 units
Manufactured in
7611 Northland Dr N, N/A, Brooklyn Park, MN, United States
Products
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1795-2024More 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
Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief