Device recall
Z-0925-2007: LIFEPAK 20 defibrillator/monitor. The device is an AC powered defibrillator…
FDA device recall · Class II · Medtronic Emergency Response Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0925-2007 |
|---|---|
| Recall event | 37864 |
| Product | LIFEPAK 20 defibrillator/monitor. The device is an AC powered defibrillator device with battery backup. The defibrillators are primarily used by healthcare providers in device user facilities such as hospitals and clinics. |
| Product code | MJK |
| Recalling firm | Medtronic Emergency Response Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 23, 2012 |
| 510(k) numbers | K012274 |
| FEI number | 3015876 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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