Medtronic recalls specific vessel cannula models due to potential unsealed sterile packing. Affected units include Model 30004 and 30003 with certain lot numbers. Consumers should check their product details.
Potential for unsealed sterile packing.
Medtronic is recalling two types of vessel cannulae that may have unsealed sterile packaging. This could lead to contamination or infection if the cannulae are used without proper sterilization.
The sterile packaging may not be properly sealed, increasing the risk of contamination. If the cannulae are used without proper sterilization, this could lead to infections or other complications during medical procedures.
Healthcare professionals and surgical teams who use these cannulae for medical procedures may be affected. Those handling the specific model numbers and lot numbers listed are most at risk.
Check for Model Numbers 30004 or 30003 with the specific lot numbers listed in the recall notice. The products were sold with GTINs and lot numbers from 2023041298 to 202306C221.
Identify the model number and lot numbers to confirm if your cannulae are affected by this recall.
Model 30004 and 30003 with specific lot numbers listed in the recall notice.
Check the model number and lot numbers against the list provided in the recall notice.
The recall does not specify a remedy, so no action is required beyond checking if your product is affected.
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-1799-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1799-2024 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.