“SenT:24/MARe-SF Ring for Sensitive Skin: Weak Skin Adhesion Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60134-sent-24-mare-sf-ring-for-sensitive-skin-weak-skin. Based on FDA recall #Z-0148-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0148-2023%22&limit=1).
SenTec AG voluntarily recalled sentec 24 / MARe-SF Multi-Site Attachment Ring Easy devices due to weak skin adhesion, according to the FDA. The recall was announced on August 22, 2022.
How to tell if you have it
Brand: SenTec
Product: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy
Batch #: 220139
Quantity: 17208 units
The hazard
The recalled devices pose a hazard of weak skin adhesion, according to the FDA.
Context
GovInfoNow's records show SenTec AG has issued four other recalls since May 2, 2019. On July 25, 2023, the company recalled a Membrane Changer due to a manufacturing defect that could affect measurement performance. A May 2, 2023 recall involved V-Sign Sensor 2 units experiencing out-of-box failure after recalibration. On December 10, 2020, the SDM Patient Monitor was recalled because it required an isolation transformer for safe home use.
How to tell if you have this one
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.
Brand
SenTec
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Batch
Look for batch number 220139 on the device.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.8 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0148-2023 (August 22, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0148-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.