Reported May 22, 2024 · Ongoing
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
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 I.M.A
- Cannulae
DLP¿ 1 mm Arteriotomy CannulaModel Number 31001
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Product as published 00613994575319Lot Numbers: 2023041320, 2023041323 00673978180465Lot Numbers: 2023041316, 2023041323 20613994575313Lot Numbers: 2023041316, 2023041318, 2023041320, 2023041323, 202305C146, 202305C154 - Amount recalled
- 7935 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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