Device recall
Z-0578-03: Life Vest (WCD 3000) Electrode Belt. Wearable Cardioverter Defibrillator…
FDA device recall · Class II · Lifecor Inc
Key facts
| Recall number (Z-number) | Z-0578-03 |
|---|---|
| Recall event | 25387 |
| Product | Life Vest (WCD 3000) Electrode Belt. Wearable Cardioverter Defibrillator. Product label 20A0051-FI. |
| Recalling firm | Lifecor Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 30, 2003 |
| PMA numbers | P010030 |
| FEI number | 3008642652 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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