Device recall
Z-0583-05: KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic…
FDA device recall · Class II · Kinetic Concepts, Inc
Key facts
| Recall number (Z-number) | Z-0583-05 |
|---|---|
| Recall event | 31207 |
| Product | KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas |
| Product code | IOQ |
| Recalling firm | Kinetic Concepts, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2008 |
| 510(k) numbers | K970468 |
| FEI number | 1625774 |
At a glance
- 1–9 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