Device recall
Z-0061-2008: Battery Pack portion of the LifeVest device. The LifeVest is a wearable…
FDA device recall · Class III · Zoll Lifecor Corporation
Key facts
| Recall number (Z-number) | Z-0061-2008 |
|---|---|
| Recall event | 44942 |
| Product | Battery Pack portion of the LifeVest device. The LifeVest is a wearable cardioverter defibrillator worn by a patient at risk for sudden cardiac arrest (SCA). |
| Product code | MVK |
| Recalling firm | Zoll Lifecor Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 13, 2008 |
| PMA numbers | P010030 |
| FEI number | 3008642652 |
At a glance
- None 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