Device recall
Z-0711-06: LIFEPAK 20 defibrillator/monitor
FDA device recall · Class II · Medtronic Emergency Response Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0711-06 |
|---|---|
| Recall event | 34947 |
| Product | LIFEPAK 20 defibrillator/monitor |
| Product code | LDD |
| Recalling firm | Medtronic Emergency Response Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 6, 2011 |
| 510(k) numbers | K012274 |
| FEI number | 3015876 |
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