Device recall
Z-1921-2017: ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology and…
FDA device recall · Class II · Roho Inc.
Key facts
| Recall number (Z-number) | Z-1921-2017 |
|---|---|
| Recall event | 76836 |
| Product | ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology and ROHO MID PROFILE Single Compartment Cushion with Sensor Ready Technology. |
| Product code | KIC |
| Recalling firm | Roho Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 10, 2019 |
| FEI number | 3008630266 |
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