Device recall
Z-1814-2013: Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2…
FDA device recall · Class II · Picis Inc.
Key facts
| Recall number (Z-number) | Z-1814-2013 |
|---|---|
| Recall event | 65666 |
| Product | Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes. |
| Product code | NSX |
| Recalling firm | Picis Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 19, 2014 |
| FEI number | 3005244943 |
At a glance
- None 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