SenTec recalls its 24/MARe-SF Multi-Site Attachment Ring for sensitive skin due to weak skin adhesion risk. Affected units have batch #220139.
Weak skin adhesion.
SenTec recalls its 24/MARe-SF Multi-Site Attachment Ring for sensitive skin because it can cause skin damage due to weak adhesion. This affects users who have the specific batch number.
The device has weak skin adhesion, which can cause skin damage or irritation, especially for sensitive or fragile skin. This risk is due to the device's design for continuous, noninvasive monitoring.
Users of the SenTec 24/MARe-SF Multi-Site Attachment Ring for sensitive skin are most at risk if they have the batch number 220139.
Check for the batch number 220139 on the product. The device is designed for sensitive/fragile skin and used in continuous, noninvasive carbon dioxide and oxygen monitoring.
Look for batch number 220139 on the device.
The recall indicates weak skin adhesion, which could cause skin damage. Users should check if they have the batch number 220139.
The recall does not specify a remedy, so users should check for the batch number 220139 and contact SenTec if needed.
The recalled product has batch number 220139 and is designed for sensitive/fragile skin for continuous, noninvasive carbon dioxide and oxygen monitoring.
We’ve drafted a message you can send SenTec to request your refund or repair — edit it as you like.
Subject: Recall Z-0148-2023 — SenTec SenTec Hello, I own a SenTec that is covered by recall Z-0148-2023 from SenTec. 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.
