Device recall
Z-2030-2009: Medtronic Physio-Control LIFEPAK CR Plus Defibrillator/Monitor. Automated…
FDA device recall · Class I · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-2030-2009 |
|---|---|
| Recall event | 53035 |
| Product | Medtronic Physio-Control LIFEPAK CR Plus Defibrillator/Monitor. Automated external defibrillator deployed primarily in public access defibrillator environments where the expected use for any one device is once every 20 months. For use on persons requiring defibrillation therapy. |
| Product code | MKJ |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 15, 2013 |
| 510(k) numbers | K011144 |
| 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