FDA Device recall Z-1597-2013
Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies
- FDA Device
- Class II
- terminated
- Published 2013-07-03
On 2013-07-03 the FDA classified a Class II recall of Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies by Rf Technologies, citing RF Technologies, Inc. has initiated a recall involving CA520 Code Alert Integrated Care Management Advanced 4-Way Care Solution . Due to a firmware error, the alarm may not be tra….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1597-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-17 |
| Published | 2013-07-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Rf Technologies |
| Distribution | US |
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.
Reason
RF Technologies, Inc. has initiated a recall involving CA520 Code Alert Integrated Care Management Advanced 4-Way Care Solution . Due to a firmware error, the alarm may not be transmitted to the system server immediately.
Identifiers
| code_info | all codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1597-2013%22
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