Device recall
Z-1656-2008: LIFEPAK 1000 defibrillator - portable battery powered semi-automated model that…
FDA device recall · Class II · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-1656-2008 |
|---|---|
| Recall event | 46918 |
| Product | LIFEPAK 1000 defibrillator - portable battery powered semi-automated model that can be operated in either of three modes: Automated external defibrillator (AED), manual defibrillator and electrocardiographic (ECG) mode. The defibrillator is intended for indoor or outdoor use in a wide variety of… |
| Product code | MKJ |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2011 |
| 510(k) numbers | K042404 |
| FEI number | 3015876 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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