FDA Device Intelligence
HomeDevice types › KMI

Monitor, Bed Patient

FDA product code KMI · Class 1 · General Hospital

1,035
Registered devices
3,238
Adverse events
32
Recalls
31
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-02-14Hill-Rom Inc.There is a software issue which may result in failure to monitor or control patient's bed exit mechanism.
2018-10-11Stanley Security Solutions IncDamaged capacitor on the printed circuit board.
2014-12-10Richard Wolf Medical Instruments Corp.The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chas
2014-08-05Curbell Medical, Inc.The firm became aware of a potential problem that was initiated by a customer complaint. After consultation with the manufacturer, it was discovered that a res
2013-05-17RF Technologies, Inc.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
2012-12-16Intel-GE Care Innovations LLCCare Innovations detected a software anomaly: During the engineering investigation into the cause of why a Wander Alert was not generated, a defect in the imple
2012-05-04Stanley Security Solutions, Inc.The monitor may fail to sound an alarm
2012-05-04Stanley Security Solutions, Inc.The monitor may fail to sound an alarm
2012-05-04Stanley Security Solutions, Inc.The monitor may fail to sound an alarm
2012-05-04Stanley Security Solutions, Inc.The monitor may fail to sound an alarm

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.