Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1501-2015 — Sentec, V-Sign Sensor 2 (REF VS-A/P/N), Reusable / Nonsterile / Waterproof, SenTec AG, CH-4106, Therwil, Switzerland. The SenTec Digital Monitoring System (SDMS) is used for continuous and non-invasive monitoring of transcutaneous carbon dioxide tension (tcPCO2), oxygen saturation (SpO2), and puls

U.S. FDA — Device Enforcement · Switzerland · 2015-03-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1501-2015
Date of alert
2015-03-25
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
SenTec AG
Product category
device
Product type
Devices
Reported risk: SenTec is voluntarily replacing V-Sign Sensors 2 due to pre-mature deterioration of a part of the PCO2 measuring unit and thus disabling PCO2-monitoring. This means that the affected sensors reach their end-of-life earlier than normally expected requiring the sensor`s replacement. There is no increased risk for the patient or operator, because the aforementioned deterioration results in the sens
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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