Device recall
Z-1407-2010: Product is a pull cord type monitor, bed patient alarm used to detect…
FDA device recall · Class II · AliMed Corporation
Key facts
| Recall number (Z-number) | Z-1407-2010 |
|---|---|
| Recall event | 54783 |
| Product | Product is a pull cord type monitor, bed patient alarm used to detect patient/resident movement. An adjustable cord is attached to both the alarm and the patient. When the patient moves beyond the length of the cord the pin is pulled and the alarm activated. |
| Product code | KMI |
| Recalling firm | AliMed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2011 |
| FEI number | 1218386 |
At a glance
- None 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