Sentec AG: Medical Device Recall in 2012 - (Recall #: Z-2199-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

SenTec, V-Sign"2 Sensors The SenTec Digital Monitoring System (SMDS) is used for continuous and noninvasive real-time monitoring of ventilation (tcPCO2) and oxygenation (SpO2).

Product Classification:

Class II

Date Initiated: July 9, 2012

Date Posted: August 22, 2012

Recall Number: Z-2199-2012

Event ID: 62589

Reason for Recall:

SenTec is recalling a number of V-Sign"2 Sensors due to a problem regarding configuration parameter writing during manufacturing.

Status: Terminated

Product Quantity: 8

Code Information:

310701 311100 311239 310996 311920 311943 311958 312132

Distribution Pattern:

Worldwide Distribution -- Nationwide including the state of Missouri,. and the countries of Germany, Spain, France, Netherlands, Australia, Belgium, Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated