Boston Scientific recalls JAGTOME RX 44-30-260-035 with material number M00573060 due to sterile barrier breach. This may compromise device sterility during medical procedures.
Sterility of device is compromised due to a sterile barrier breach
Boston Scientific is recalling a specific JAGTOME RX device model because a sterile barrier breach could compromise sterility during medical procedures. This means the device might not be sterile when used, which is critical for patient safety.
The device has a sterile barrier that was breached, meaning it may not be sterile when used. This could lead to infections or other complications during medical procedures if the device is not properly sterilized.
Medical professionals using the JAGTOME RX device for procedures are most at risk. Patients receiving the device could be affected if sterility is compromised.
Check for the model number JAGTOME RX 44-30-260-035 with material number M00573060. The device was sold with specific lot numbers including 27522394 through 28289453.
Identify the model number JAGTOME RX 44-30-260-035 and material number M00573060 on the device.
The sterile barrier in the device was breached, which could compromise sterility during medical procedures.
The recall record does not specify a remedy, so contact Boston Scientific directly for guidance.
Check for the model number JAGTOME RX 44-30-260-035 with material number M00573060 and lot numbers listed in the recall.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0775-2022 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0775-2022 from Boston Scientific. 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.