Device recall
Z-0886-04: LIFEPAK 500 automated external defibrillator
FDA device recall · Class II · Medtronic Physio Control Corp
Key facts
| Recall number (Z-number) | Z-0886-04 |
|---|---|
| Recall event | 28727 |
| Product | LIFEPAK 500 automated external defibrillator |
| Product code | MKJ |
| Recalling firm | Medtronic Physio Control Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 6, 2005 |
| 510(k) numbers | K012428 |
| 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