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

Products covered by this recall
Model / numberProduct 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 / numberBarcodesProduct 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.