Device recall
Z-3276-2026: Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000…
FDA device recall · Class II · Volcano Corp
Key facts
| Recall number (Z-number) | Z-3276-2026 |
|---|---|
| Recall event | 99730 |
| Product | Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA |
| Product code | IYO |
| Recalling firm | Volcano Corp |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K253714 |
| FEI number | 3008363989 |
At a glance
- 1–9 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