Medtronic Perfusion Systems recalls specific arterial cannula models due to incorrect labeling in seven lots. This may cause confusion in medical use. Affected units include model 77422 (22 Fr) and 77418 (18 Fr) with listed lot numbers.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Medtronic Perfusion Systems is recalling certain arterial cannula models (77422 and 77418) because they have incorrect labeling in seven manufactured lots. This could lead to confusion during medical procedures, potentially affecting patient safety.
Incorrect labeling in seven specific lots of arterial cannulas could lead to confusion during medical procedures. This might result in using the wrong cannula size or type, potentially affecting patient safety.
Healthcare professionals using these specific arterial cannula models are most at risk. Patients receiving procedures with these cannulas may be affected if the labeling error causes incorrect use.
Check for model numbers 77422 (22 Fr) or 77418 (18 Fr) with lot numbers 2022041038 or 2023020934. The UDI-DI numbers listed in the recall are 20763000135618 and 20643169485970.
Verify the model number and lot number on the cannula to confirm if it is affected by this recall.
Model numbers 77422 (22 Fr) and 77418 (18 Fr) with specific lot numbers 2022041038 and 2023020934.
Check the model number and lot number on the cannula. Affected units have model 77422 with lot 2023020934 or model 77418 with lot 2022041038.
The recall does not specify a remedy, so contact Medtronic Perfusion Systems directly for guidance.
We’ve drafted a message you can send Medtronic Perfusion Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0985-2025 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-0985-2025 from Medtronic Perfusion Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
