Recall Z-1106-2017— Philips Electronics North America Corporation
Class II · Terminated
Class II FDA medical device recall by Philips Electronics North America Corporation, initiated 2016-12-27, terminated 2020-10-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Philips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S-E in use with IntelliVue Information Center iX or Classic Information Center. Reason: May experience a loss of centralized monitoring..
- Recalling firm
- Philips Electronics North America Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-12-27
- Terminated
- 2020-10-08
- Firm location
- Andover, MA, United States
Product description
Philips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S-E in use with IntelliVue Information Center iX or Classic Information Center
Reason for recall
May experience a loss of centralized monitoring.
Data sourced from openFDA. This site is unofficial and independent of the FDA.