Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled by Ansar Group, Inc. Dba Ansar Medical Technologies, Inc Due to The blood pressure (BP) circuit occasionally fails to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ansar Group, Inc. Dba Ansar Medical Technologies, Inc directly.
Affected Products
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.
Quantity: 351
Why Was This Recalled?
The blood pressure (BP) circuit occasionally fails to inflate the blood pressure cuff and the BP circuit fails to activate, resulting in no BP measured.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ansar Group, Inc. Dba Ansar Medical Technologies, Inc
Ansar Group, Inc. Dba Ansar Medical Technologies, Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report