Device recall
Z-0562-05: LIFEPAK 500 AED.
FDA device recall · Class I · Medtronic Emergency Response Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0562-05 |
|---|---|
| Recall event | 31111 |
| Product | LIFEPAK 500 AED. |
| Product code | MKJ |
| Recalling firm | Medtronic Emergency Response Systems, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 21, 2006 |
| FEI number | 3015876 |
At a glance
- None 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