Device recall
Z-0271-04: Philips Digital Diagnost VT
FDA device recall · Class II · Philips Medical Systems Sales & Service Region No. America
Key facts
| Recall number (Z-number) | Z-0271-04 |
|---|---|
| Recall event | 27839 |
| Product | Philips Digital Diagnost VT |
| Product code | KPR |
| Recalling firm | Philips Medical Systems Sales & Service Region No. America |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2005 |
| FEI number | 1000524572 |
At a glance
- None 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