Device recall
Z-0294-2018: LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e…
FDA device recall · Class I · Physio-Control, Inc.
Key facts
| Recall number (Z-number) | Z-0294-2018 |
|---|---|
| Recall event | 78574 |
| Product | LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in the hospital, physician s office, and clinic setting by personnel who are authorized by a physician/medical director. It is intended for use on a crash cart as well as for portable… |
| Product code | MKJ |
| Recalling firm | Physio-Control, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 1, 2024 |
| 510(k) numbers | K130454 |
| 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