FDA-Device2024-09-18Class II
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Hazard
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
Sold states
Worldwide distribution - US Nationwide and the countries of Cambodia, Greece, Ireland, Italy, Saudi Arabia, Switzerland, United Kingdom, Viet Nam.
Affected count
290 units
Manufactured in
7611 Northland Dr N, Brooklyn Park, MN, United States
Products
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3128-2024More 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
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