Device recall
Z-2650-2026: Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64…
FDA device recall · Class II · PHILIPS MEDICAL SYSTEMS
Key facts
| Recall number (Z-number) | Z-2650-2026 |
|---|---|
| Recall event | 99352 |
| Product | Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades |
| Product code | JAK |
| Recalling firm | PHILIPS MEDICAL SYSTEMS |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K250648 |
| FEI number | 3017726341 |
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