Sotera Wireless, Inc.: Medical Device Recalls in 2013

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Sotera Wireless, Inc. in 2013. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014 The ViSi Mobile Monitoring System is intended for use by clinicians and medically qualified personnel for single or multi-parameter vital signs monitoring of adult patients.
ViSi Mobile Monitor, Catalog No. 92-10010 The ViSi Mobile Monitoring System is intended for use by clinicians and medically qualified personnel for single or multi-parameter vital signs monitoring of adult patients.