Device recall
Z-1894-2017: Sonesta S2; Article numbers: 525-S2-110V and 525S2-220V
FDA device recall · Class II · Sonesta Medical Ab
Key facts
| Recall number (Z-number) | Z-1894-2017 |
|---|---|
| Recall event | 77075 |
| Product | Sonesta S2; Article numbers: 525-S2-110V and 525S2-220V |
| Product code | MMZ |
| Recalling firm | Sonesta Medical Ab |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 20, 2019 |
| FEI number | 3010496070 |
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