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FDAFDA · Food and drugs·Recall number Z-0433-2013

SenTec V-Sign Membrane Changer (VS-MC), 9 pieces. The SenTec V-Sign Membrane Changer is indicated for use with the V-Sign Sensor only. The V-sign Sensor is indicated for use with the SenTec Digital Monitor when continuous non-invasive monitoring of carbon dioxide tension, oxygen saturation, and pulse rate are required for adult and pediatric patients.

Published November 28, 2012 · Recall initiated: November 5, 2012

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

A manufacturing defect was observed for the membrane changer insert that does not allow electrolyte to be present under the new membrane. The PCO2 performance of a sensor without electrolyte will be deteriorated.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Sentec AG
Distributor
Distributed only in MO.
Lot
Lot numbers: 1CF5, 1D21, 1D60, 1DC6, 1DED, 1E0D
Risk classification
Class II
Area (FDA)
device
Country
Switzerland

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