Device recall
Z-1597-2013: Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF…
FDA device recall · Class II · RF Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1597-2013 |
|---|---|
| Recall event | 65361 |
| Product | Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies. This product is used to alert caregivers when a patient at risk for falls is leaving a bed or chair. |
| Product code | KMI |
| Recalling firm | RF Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 3, 2013 |
| FEI number | 3002286578 |
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