Device recall
Z-0920-05: Carroll Healthcare brand Spirit bed; models BH2180-111AE, BH2180-111PE and…
FDA device recall · Class II · Carroll Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-0920-05 |
|---|---|
| Recall event | 32093 |
| Product | Carroll Healthcare brand Spirit bed; models BH2180-111AE, BH2180-111PE and BH2180-111FE. |
| Product code | FNL |
| Recalling firm | Carroll Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2005 |
| FEI number | 3002706498 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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