Reported May 22, 2024 · Ongoing
Medtronic DLP Coronary Ostial Cannulae, Model Number 30050
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 DLP Coronary Ostial Cannulae, Model Number 30050
- Lot codes and dates
- GTIN 00613994576019
- Lot Numbers
2023070529GTIN 20613994576013
- Lot Numbers2023070529
- Amount recalled
- 250 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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