Medtronic Perfusion Systems recalls Select Series Angled Tip Arterial Cannula (Model 72422) due to incorrect labeling in seven lots. Affected units may have safety risks.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Medtronic Perfusion Systems is recalling certain models of Angled Tip Arterial Cannula (Model 72422) because of incorrect labeling in seven specific lots. This could lead to safety risks if the labeling is not accurate.
Incorrect labeling could lead to confusion about the product's specifications, potentially causing errors in medical procedures. This might result in improper use or incorrect application of the cannula.
Healthcare professionals who use the recalled cannulae are likely affected. Patients receiving these cannulae during medical procedures may be at risk.
Check for Model Number 72422 (22 Fr) with specific lot numbers: 2023071075 and 202309C075. The product was manufactured in specific lots with UDI-DI codes starting with 20643169485970.
Look for the model number 72422 (22 Fr) and lot numbers 2023071075 or 202309C075 on the product.
The model number is 72422 (22 Fr).
Lots 2023071075 and 202309C075 are affected.
Check for the model number 72422 (22 Fr) with lot numbers 2023071075 or 202309C075.
We’ve drafted a message you can send Medtr: 1.2.3 to request your refund or repair — edit it as you like.
Subject: Recall Z-0986-2025 — Medtr: 1.2.3 Medtr: 1.2.3 Hello, I own a Medtr: 1.2.3 that is covered by recall Z-0986-2025 from Medtr: 1.2.3. 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.
