Device recall
Z-0888-04: KCI Therapulse II Air Suspension Therapy Bed, manufactured by Kinetic Concepts…
FDA device recall · Class II · Kinetic Concepts, Inc
Key facts
| Recall number (Z-number) | Z-0888-04 |
|---|---|
| Recall event | 28683 |
| Product | KCI Therapulse II Air Suspension Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX 78219. Model number 227080 |
| Product code | INX |
| Recalling firm | Kinetic Concepts, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2005 |
| FEI number | 1625774 |
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