Device recall
Z-0676-2008: Philips Medical Systems -- Cardiac Viewer or Pulmonary Viewer software…
FDA device recall · Class II · Phillips Nuclear Medicine
Key facts
| Recall number (Z-number) | Z-0676-2008 |
|---|---|
| Recall event | 45329 |
| Product | Philips Medical Systems -- Cardiac Viewer or Pulmonary Viewer software application version 2.0 in use with Precedence SPECT/CT System and all CT EBW workstations using software version 3.5. Philips Nuclear Medicine, Milpitas, CA 95035 |
| Product code | KPS |
| Recalling firm | Phillips Nuclear Medicine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2009 |
| 510(k) numbers | K041218 |
| FEI number | 1525965 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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