Device recall
Z-1949-2024: HA FlexTrak-Patient transport functionality to transport the patient from the…
FDA device recall · Class II · Philips North America Llc
Key facts
| Recall number (Z-number) | Z-1949-2024 |
|---|---|
| Recall event | 94603 |
| Product | HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006412 |
| Product code | LNH |
| Recalling firm | Philips North America Llc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K213583 |
| FEI number | 3016618143 |
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