Medtronic recalls specific cardioplegia adapter models due to potential unsealed sterile packing. Affected units include Model Numbers 25009, 25010, 14003, 14000, 11001G, 13002, and 10710 with specific lot numbers. Consumers should check their units and contact Medtronic for details.
Potential for unsealed sterile packing.
Medtronic is recalling several cardioplegia adapter models that may have unsealed sterile packaging. This could lead to contamination during medical procedures, posing a risk to patient safety.
The adapters may have unsealed sterile packaging, which can lead to contamination during medical procedures. This contamination could potentially harm patients during cardiac surgery by introducing pathogens or other contaminants into the sterile field.
Healthcare professionals using these adapters during cardiac surgery are most at risk. Patients undergoing surgery with these specific models could be affected if the sterile packaging is compromised.
Check for model numbers 25009, 25010, 14003, 14000, 11001G, 13002, or 10710 with specific lot numbers listed in the recall notice. These adapters are used in cardiac surgery procedures.
Identify the model number and lot number on your Medtronic Cardioplegia Adapter to see if it matches the recalled items.
Reach out to Medtronic Perfusion Systems for guidance on whether your adapter is affected and what steps to take next.
The recall includes Model Numbers 25009, 25010, 14003, 14000, 11001G, 13002, and 10710 with specific lot numbers listed in the notice.
Check the model number and lot number on your adapter against the list provided in the recall notice.
Contact Medtronic Perfusion Systems for instructions on how to proceed with the affected adapter.
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-1801-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1801-2024 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.
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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.
