Device recall
Z-3160-2011: Picis ED PulseCheck-Software, transmission & storage, patient data Service Pack…
FDA device recall · Class II · Picis Inc.
Key facts
| Recall number (Z-number) | Z-3160-2011 |
|---|---|
| Recall event | 59737 |
| Product | Picis ED PulseCheck-Software, transmission & storage, patient data Service Pack v5.0 L and M This product is a non-alarming software patient information system that compiles an electronic medical record utilizing commonly available hardware. A patient record is populated with information from… |
| Product code | NSX |
| Recalling firm | Picis Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2013 |
| 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