Device recall
Z-2268-2014: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor system. The…
FDA device recall · Class II · Ansar Group, Inc. Dba Ansar Medical Technologies, Inc
Key facts
| Recall number (Z-number) | Z-2268-2014 |
|---|---|
| Recall event | 68735 |
| Product | 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… |
| Product code | DRT |
| Recalling firm | Ansar Group, Inc. Dba Ansar Medical Technologies, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 10, 2015 |
| 510(k) numbers | K941252 |
| FEI number | 3000210032 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database