Device recall
Z-1257-2017: The LIFEPAK 1000 defibrillator is intended for use by personnel who are…
FDA device recall · Class I · Physio-Control, Inc.
Key facts
| Recall number (Z-number) | Z-1257-2017 |
|---|---|
| Recall event | 76252 |
| Product | The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator. |
| Product code | MKJ |
| Recalling firm | Physio-Control, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 22, 2019 |
| 510(k) numbers | K122600 |
| 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