Reported May 22, 2024 · Ongoing
Medtronic Venous Cannulae
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 Venous Cannulae
9 of 9 products
| Model / number | Product as published |
|---|---|
MC2¿ | 36 Fr. Single Stage Venous Cannula, Model Number 66236, z) |
MC2¿ | 28/36 Fr. Two Stage Venous Cannula, Model Number 91228, aa) |
MC2¿ | 29/37 Fr. Two Stage Venous Cannula, Model Number 91229C, bb) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263, cc) |
MC2¿ | 32/40 Fr. Two Stage Venous Cannula, Model Number 91240C, dd) MC2¿ 32/40 Fr. Two Stage Venous Cannula, Model Number 91263C, ee) |
MC2¿ | 34/46 Fr. Two Stage Venous Cannula, Model Number 91246, ff) |
MC2¿ | 34/46 Fr. Two Stage Venous Cannula, Model Number 91246C, gg) |
MC2¿ | 36/46 Fr. Two Stage Venous Cannula, Model Number 91236C, hh) MC2¿ 36/51 Fr. Two Stage Venous Cannula, Model Number 91251, ii) |
VC2" | 36/51 Fr. Two Stage Venous Cannula, Model Number 91251C, jj) |
VC2" | 34/38 Fr. Venous Cannula, Model Number 93438, kk) |
- Lot codes and dates
49 of 49 products
Products covered by this recall Model / number Barcodes Product as published 20613994879435Model Number 68120, , Lot Numbers: 2023041436 00613994879417Model Number 68124, , Lot Numbers: 2023041441, 2023041448 00681490466349Model Number 68124, , Lot Numbers: 2023041441, 2023041448 20613994879411Model Number 68124, , Lot Numbers: 2023041441, 2023041448, 202306C008 00613994879394Model Number 68128, , Lot Numbers: 2023041040 00681490466363Model Number 68128, , Lot Numbers: 2023041388 20613994879398Model Number 68128, , Lot Numbers: 2023041040, 2023041388, 202306C010, 202306C011 20613994879381Model Number 68130, , Lot Numbers: 2023041390, 202308C131 20613994879367Model Number 68134, , Lot Numbers: 2023041431 00613994879325Model Number 67312, , Lot Numbers: 2023041423 00673978184180Model Number 67312, , Lot Numbers: 2023040074 20613994879329Model Number 67312, , Lot Numbers: 2023040073, 2023040074, 2023041423 00613994879301Model Number 67316, , Lot Numbers: 2023040076, 2023041416 20613994879305Model Number 67316, , Lot Numbers: 2023040076, 2023041416, 202305C264 00613994879301Model Number 67516, , Lot Numbers: 2023040076, 2023041416 20613994879305Model Number 67516, , Lot Numbers: 2023040076, 2023041416, 202305C264 00613994878526Model Number 66118, , Lot Numbers: 2023041014 20613994878520Model Number 66118, , Lot Numbers: 2023041014, 2023041015 00613994879295Model Number 67318, , Lot Numbers: 2023040077 00673978184241Model Number 67318, , Lot Numbers: 2023040077, 2023041391 - Amount recalled
- 17221 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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