Device recall
Z-0176-05: Alto implantable cardioverter defibrillator
FDA device recall · Class II · ela Medical Llc
Key facts
| Recall number (Z-number) | Z-0176-05 |
|---|---|
| Recall event | 30273 |
| Product | Alto implantable cardioverter defibrillator |
| Product code | LWS |
| Recalling firm | ela Medical Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 14, 2005 |
| PMA numbers | P980049, P980049/S3, P980049/S6 |
| FEI number | 2182863 |
At a glance
- None 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