SUNBEAM SWM6000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-02-27 for SUNBEAM SWM6000 manufactured by Sunbeam Products, Inc..

Event Text Entries

[184632569] An insurance company is making a subrogation claim under case reference number (b)(4) and alleging that a humidifier was the cause of a fire that damaged its insured's property. There was not a report of personal injury with this incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010341502-2020-00017
MDR Report Key9763681
Report SourceOTHER
Date Received2020-02-27
Date of Report2020-02-27
Date of Event2019-12-29
Date Added to Maude2020-02-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMICHAEL MILES
Manufacturer Street303 NELSON AVE.
Manufacturer CityNEOSHO, MO
Manufacturer CountryUS
Manufacturer Phone4557441
Manufacturer G1CHUZHOU DONLIM ELECTRICAL APPLIANCES CO.,LTD.
Manufacturer StreetNO.1777 YANGZI EAST ROAD
Manufacturer CityCHUZHOU, ANHUI 239000
Manufacturer CountryCH
Manufacturer Postal Code239000
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSUNBEAM
Generic NameHUMIDIFIER
Product CodeKFZ
Date Received2020-02-27
Model NumberSWM6000
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSUNBEAM PRODUCTS, INC.
Manufacturer Address2381 EXECUTIVE CENTER DR. BOCA RATON, FL US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-27

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