Device recall
Z-0929-2024: BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit…
FDA device recall · Class I · Philips North America
Key facts
| Recall number (Z-number) | Z-0929-2024 |
|---|---|
| Recall event | 93767 |
| Product | BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4x4 digit format 2170-3000A 2170-3001A 2170-3002A 2170-3003A |
| Product code | KPS |
| Recalling firm | Philips North America |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K062298 |
| FEI number | 3006648320 |
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