Reported May 22, 2024 · Ongoing
Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt…
Medtronic Perfusion Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Perfusion Systems · 7611 Northland Dr N · Brooklyn Park, MN · 55428-1088
Is this the product you have?
- Medtronic Vessel Cannulae
a) DLP¿ 2 mm Vessel Cannula Blunt TipModel Number 30004b) DLP¿ 3 mm Vessel Cannula Blunt TipModel Number 30003
- Lot codes and dates
4 of 4 products
Products covered by this recall Model / number Product as published 00613994646156Model Number 30004, , Lot Numbers: 2023041305 00673978179841Model Number 30004, , Lot Numbers: 2023041300 20613994646150Model Number 30004, , Lot Numbers: 2023041300, 2023041305, 202306C194 20613994646174Model Number 30003, , Lot Numbers: 2023041298, 202306C221 - Amount recalled
- 5719 units
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Why it was recalled
Potential for unsealed sterile packing.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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