Device recall
Z-0863-2019: LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15…
FDA device recall · Class I · Physio-Control Inc
Key facts
| Recall number (Z-number) | Z-0863-2019 |
|---|---|
| Recall event | 81939 |
| Product | LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. The LP15 monitor/defibrillator is intended… |
| Product code | MKJ |
| Recalling firm | Physio-Control Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 18, 2024 |
| 510(k) numbers | K142430 |
| 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