Device recall
Z-0988-2014: Siemens Prisma 2K Hearing Aid Product Usage: A behind the ear (BTE) hearing aid…
FDA device recall · Class II · Siemens Hearing Instruments, Inc
Key facts
| Recall number (Z-number) | Z-0988-2014 |
|---|---|
| Recall event | 67241 |
| Product | Siemens Prisma 2K Hearing Aid Product Usage: A behind the ear (BTE) hearing aid developed for pediatric patients. |
| Product code | LEZ |
| Recalling firm | Siemens Hearing Instruments, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 2017 |
| FEI number | 2217809 |
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