Device recall
Z-0185-2012: The LIFEPAK 20 defibrillator/monitor is an AC powered external defibrillator…
FDA device recall · Class II · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-0185-2012 |
|---|---|
| Recall event | 60202 |
| Product | The LIFEPAK 20 defibrillator/monitor is an AC powered external defibrillator with battery backup used by healthcare providers in hospital and clinic settings. Affected Product Part Numbers: 3202487-000 thru -012, 3202487-014 thru -027, 3203487-029 thru -039, 3202488-000 thru -019, U3202487-000… |
| Product code | LDD |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 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