Medtronic recalls specific arterial cannulae models due to potential unsealed sterile packing. Affected items include various 20-24 Fr sizes with model numbers 77006-87222. Consumers should check model numbers and lot numbers listed to determine if their product is affected.
Potential for unsealed sterile packing.
Medtronic is recalling certain arterial cannulae products that may have unsealed sterile packaging. This could lead to contamination or infection if used improperly. Affected items include specific model numbers and lot numbers listed in the recall notice.
The sterile packaging may not be properly sealed, which could allow contamination. If the packaging is compromised, the cannulae might become infected or contaminated during medical procedures, posing a risk to patients.
Medical professionals and hospitals that use these arterial cannulae products are most likely affected. Patients using these cannulae during procedures could be at risk if the sterile packaging is compromised.
Check the model number and lot number on the packaging. Affected items include specific arterial cannulae models with numbers ranging from 77006 to 87222, and lot numbers listed in the recall notice.
Review the model number and lot number on the packaging to see if it matches the affected items listed in the recall.
No, only specific models with model numbers 77006-87222 and the listed lot numbers are affected.
Check the model number and lot number on the packaging against the list provided in the recall notice.
The recall does not specify a remedy, so contact Medtronic directly for further instructions.
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-1793-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1793-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
