← DeviceEvents
HomeDevice Adverse Events

FR3, REFURB ECG AED, LANGUAGE CONFIGURAB Adverse Event — Malfunction (MDR 3030677-2020-00715)

FR3, REFURB ECG AED, LANGUAGE CONFIGURAB Adverse Event — Malfunction (MDR 3030677-2020-00715) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FR3, REFURB ECG AED, LANGUAGE CONFIGURAB; Generic name: AED; Manufacturer: PHILIPS MEDICAL SYSTEMS.

DeviceFR3, REFURB ECG AED, LANGUAGE CONFIGURAB
Generic nameAED
ManufacturerPHILIPS MEDICAL SYSTEMS
Report number3030677-2020-00715
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCONSUMER, FOREIGN
NarrativeIT HAS BEEN REPORTED THAT THE DEVICE SPEAKERS ARE NOT FUNCTIONING PROPERLY.
SourceopenFDA MAUDE (device adverse events)

🔍 Search all device adverse events →