Boston Scientific recalls JAGTOME RX 39-30-260-025 with sterile barrier breach. This could 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 due to a sterile barrier breach that could compromise sterility during medical procedures. This is serious because medical devices must be sterile to prevent infections.
The sterile barrier breach means the device might not be sterile when used. This could lead to infections during medical procedures if the device is not properly sterilized after the breach.
Medical professionals using this 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 39-30-260-025 and material number M00573100. The device was sold with lot numbers 27857328 and GTIN 8714729776529.
Identify the model number JAGTOME RX 39-30-260-025 and material number M00573100.
The recall states the sterile barrier may be breached, so it is not safe to use without checking the recall status.
The recall does not specify a remedy, so contact Boston Scientific for guidance.
Check for the model number JAGTOME RX 39-30-260-025 and material number M00573100.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0771-2022 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0771-2022 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.
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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.
