Device recall
Z-0011-2015: Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity…
FDA device recall · Class II · Nemschoff Chairs, Inc.
Key facts
| Recall number (Z-number) | Z-0011-2015 |
|---|---|
| Recall event | 69092 |
| Product | Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS: 792-12. Designed to provide patient comfort during patient treatment sessions. The chair may include a manual control reclining mechanism. Customer configurable models are also… |
| Product code | INM |
| Recalling firm | Nemschoff Chairs, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 24, 2015 |
| FEI number | 3001591966 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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