Device recall
Z-1664-2011: LUCAS 2 Chest Compression System. The device's Instruction for Use is labeled in…
FDA device recall · Class III · Jolife AB
Key facts
| Recall number (Z-number) | Z-1664-2011 |
|---|---|
| Recall event | 57967 |
| Product | LUCAS 2 Chest Compression System. The device's Instruction for Use is labeled in part: "LUCAS 2 Chest Compression System***jolife***www.lucas-cpr.com***a product by JOLIFE***MANUFACTURER, MAIN OFFICE JOLIFE AB Scheelevagen 17 SE-223 70 LUND Sweden***www.jolife.com***". Designed to uninterrupted… |
| Product code | DRM |
| Recalling firm | Jolife AB |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 24, 2012 |
| 510(k) numbers | K090422 |
| 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