Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:128581

Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor system. The ANX 3.0 system is comprised of these components. 1. Patient Physiological Monitor, 2. Laptop Computer, 3. Stand w/wheels, 4. Patient cables, 5. Software components (Respiratory and Cardiac Spectral Frequency Signal Processor). The different monitor components that can be used in the system are one of the following per system are as follows: Patient Physiological Monitors used: CJPS Vital Pro, Zoe Medical Nightingale Monitoring system, Ivy Biomedical model 405P, Software components: Ansar ANS C 3000. The device is also referred to as the ANS-C3000.

Official recall number

Z-2268-2014

Evidence summary

Product code
DRT
Recall status
Terminated
Event initiated
July 01, 2014
Root cause
Unknown/Undetermined by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2268-2014

Field note

Send feedback

We'll only use this to respond to your feedback.