Sotera Wireless, Inc. Recall: ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No
Sotera Wireless, Inc. Recall: ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Sotera Wireless, Inc.; Product: ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014 The ViSi Mobile Monitoring System is intende
| Recalling firm | Sotera Wireless, Inc. |
|---|---|
| Product | 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. |
| Reason for recall | Sotera Wireless, Inc. is recalling the ViSi Mobile Monitoring System due to the potential for the Chest Sensor to cause a blister wound. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US distribution including CA and UT. |
| Recall initiated | 20130523 |
| Recall number | Z-1818-2013 |
| Category | device |
| State | CA |
| Country | United States |
$29/mo
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