Recall Z-1597-2013— RF Technologies, Inc.
Class II · Terminated
Class II FDA medical device recall by RF Technologies, Inc., initiated 2013-05-17, terminated 2013-12-03. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- RF Technologies, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-05-17
- Terminated
- 2013-12-03
- Firm location
- Brookfield, WI, United States
Product description
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 for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.