Device recall
Z-0919-05: Carroll Healthcare brand Arro bed models BA3180-151 AE, BA3180-151 PE…
FDA device recall · Class II · Carroll Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-0919-05 |
|---|---|
| Recall event | 32093 |
| Product | Carroll Healthcare brand Arro bed models BA3180-151 AE, BA3180-151 PE, BA3180-151 FE, BA3180-171 AE, BA3180-171 FE and BA3180-171 FE. |
| 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