Device recall
Z-0990-03: CLINITRON UP-LIFT Air Fluidized Therapy unit.
FDA device recall · Class II · Hill-Rom Manufacturing, Inc.
Key facts
| Recall number (Z-number) | Z-0990-03 |
|---|---|
| Recall event | 26486 |
| Product | CLINITRON UP-LIFT Air Fluidized Therapy unit. |
| Product code | INX |
| Recalling firm | Hill-Rom Manufacturing, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2004 |
| 510(k) numbers | K920112 |
| FEI number | 1045510 |
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