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 pulse rate (PR).
FDA Recall Z-1501-2015 · Posted 2015-04-22
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Recalling FirmSenTec AG
Recall StatusTerminated
Product CodeLKD
Date Initiated2015-03-25
Date Terminated2016-02-05
Product Quantity129 US, 59 OUS
Reason for Recall
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
Firm Action
Sentec sent an Important Information letter via email dated March 25, 2015. The letter described the problem and the product involved in the recall. Customers were instructed to locate the affected sensors at their end-customers and replace them with the new sensors. Replaced sensors are to be returned to SenTec. For questions contact SenTec at + 41 61 726 97 60.
Consignee was sent an emai in regard to the recall being expanded. The email was sent on May 08, 2014. The email informed the consignee of the additional lot being affected and provided a list of the serial number of V-Sign Sensors to be replaced.
Root Cause
Under Investigation by firm
Distribution Pattern
US Distribution to the state of : MO
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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