Device recall
Z-1395-2017: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable…
FDA device recall · Class II · MED-EL Elektromedizinische Gereate, Gmbh
Key facts
| Recall number (Z-number) | Z-1395-2017 |
|---|---|
| Recall event | 76503 |
| Product | SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery Pack, which is an external battery pack used to power one MED-EL SONNET control unit. It can be worn on the upper body or the hip using different SONNET Mini Battery Pack Cable lengths… |
| Product code | ISM |
| Recalling firm | MED-EL Elektromedizinische Gereate, Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 4, 2017 |
| PMA numbers | P000025, P000025S087 |
| FEI number | 3000249315 |
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