Device recall
Z-1410-2010: Biphasic LIFEPAK 15 Monitor/Defibrillator. Manufactured by Physio-Control Inc…
FDA device recall · Class I · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-1410-2010 |
|---|---|
| Recall event | 54894 |
| Product | Biphasic LIFEPAK 15 Monitor/Defibrillator. Manufactured by Physio-Control Inc., a division of Medtronic, Inc. Redmond, Washington USA. The LIFEPAK 15 monitor/defibrillator is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient… |
| Product code | MKJ |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 3, 2012 |
| 510(k) numbers | K082937 |
| 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