Device recall
Z-1132-2012: Clinitron Rite Hite Bed headboard and foot side rails. The Clinitron Rite Hite…
FDA device recall · Class III · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-1132-2012 |
|---|---|
| Recall event | 60888 |
| Product | Clinitron Rite Hite Bed headboard and foot side rails. The Clinitron Rite Hite Air Fluidized Therapy Unit is a patient management system that combines air fluidized therapy and low airloss therapy technologies together on a low-height frame. The lower body section provides air fluidized therapy, and… |
| Product code | INX |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 5, 2012 |
| 510(k) numbers | K964223 |
| FEI number | 1824206 |
At a glance
- 1–9 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