Device recall
Z-0807-2024: Achieva 1.5T, Model No. 781178, 781196, 781296
FDA device recall · Class III · Philips North America
Key facts
| Recall number (Z-number) | Z-0807-2024 |
|---|---|
| Recall event | 93788 |
| Product | Achieva 1.5T, Model No. 781178, 781196, 781296 |
| Product code | LNI |
| Recalling firm | Philips North America |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K193215 |
| FEI number | 3006648320 |
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