Device recall
Z-2161-2026: LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011…
FDA device recall · Class II · Jolife AB
Key facts
| Recall number (Z-number) | Z-2161-2026 |
|---|---|
| Recall event | 98417 |
| Product | LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression… |
| Product code | DRM |
| Recalling firm | Jolife AB |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K090422, K161768 |
| FEI number | 3005445717 |
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