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Sotera Wireless Recalls
2 recalls on record · August 7, 2013 to August 7, 2013 · Medical Devices
August 7, 2013Medical DevicesFDA
Sotera Wireless, Inc. recalls ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014 The ViSi Mobile Monitoring System is intended
Hazard: Sotera Wireless, Inc. is recalling the ViSi Mobile Monitoring System due to the potential for the Chest Sensor to cause a blister wound.
August 7, 2013Medical DevicesFDA
Sotera Wireless, Inc. recalls ViSi Mobile Monitor, Catalog No. 92-10010 The ViSi Mobile Monitoring System is intended for use by clinicians and med
Hazard: Sotera Wireless, Inc. is recalling the ViSi Mobile Monitoring System due to the potential for the Chest Sensor to cause a blister wound.