Device recall
Z-1131-2012: Clinitron At Home Bed headboard and foot side rails. The Clinitron At Home Air…
FDA device recall · Class III · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-1131-2012 |
|---|---|
| Recall event | 60888 |
| Product | Clinitron At Home Bed headboard and foot side rails. The Clinitron At Home Air Fluidized Therapy Unit provides a pressure-relieving sleep surface for patients in the home environment. It helps enable patients with pressure sores to heal their wounds |
| 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