Device recall
Z-1998-2025: LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing…
FDA device recall · Class II · Jolife AB
Key facts
| Recall number (Z-number) | Z-1998-2025 |
|---|---|
| Recall event | 96729 |
| Product | LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness. |
| 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