Device recall
Z-2341-2008: LIFEPAK CR Plus Automated External Defibrillator. Device is primarily deployed…
FDA device recall · Class I · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-2341-2008 |
|---|---|
| Recall event | 49396 |
| Product | LIFEPAK CR Plus Automated External Defibrillator. Device is primarily deployed in Public Access Defibrillator (PAD). It is a small lightweight device intended for use by minimally trained responders to treat victims of sudden cardiac arrest... Product is capable of 30 full discharges. Labeling on… |
| Product code | MJK |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 8, 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
- 1–9 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