Medtronic recalls pediatric blood collection sets due to potential bacterial endotoxin levels that could cause acute inflammatory responses in patients.
Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.
Medtronic is recalling pediatric blood collection sets that may contain elevated bacterial endotoxins. This could lead to acute inflammatory responses in patients exposed to the endotoxins.
The recalled sets may have higher than safe levels of bacterial endotoxins. When patients are exposed to these endotoxins, they can develop an acute inflammatory response, which is a serious medical reaction.
Patients receiving the recalled pediatric blood collection sets during surgery are at risk. Healthcare providers using these sets for extracorporeal circulation are also affected.
Check for the model number M484901D on the product label. The product was sold with lot number 220906731.
Look for the model number M484901D and lot number 220906731 on the product.
The model number is M484901D.
The lot number is 220906731.
The product may contain elevated levels of bacterial endotoxins that could cause acute inflammatory responses in patients.
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-1198-2021 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1198-2021 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.
