Device recall
Z-0167-2014: Aquatec Ocean VIP, Aquatec Ocean Dual-VIP, Aquatec Ocean E-VIP mobile shower and…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-0167-2014 |
|---|---|
| Recall event | 66461 |
| Product | Aquatec Ocean VIP, Aquatec Ocean Dual-VIP, Aquatec Ocean E-VIP mobile shower and toilet commode with tilting function. Mobile shower and toilet commode with tilting function |
| Product code | INN |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2014 |
| FEI number | 1525712 |
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