CONAIR BMS3

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-03-21 for CONAIR BMS3 manufactured by Conair Corporation.

Event Text Entries

[70425867] On 3/6/2017 - we have requested the device to returned to the manufacturer. To date, we have not received the device.
Patient Sequence No: 1, Text Type: N, H10


[70425868] On 3/6/2017 - the consumer claims was laying on the product. The consumer realized the next morning to have received burned marks and a blister. Medical attention was not required.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222304-2017-00013
MDR Report Key6420327
Report SourceCONSUMER
Date Received2017-03-21
Date of Report2017-02-24
Date of Event2017-02-21
Date Added to Maude2017-03-21
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 Street1 CUMMINGS POINT RD
Manufacturer CitySTAMFORD CT 06902
Manufacturer CountryUS
Manufacturer Postal06902
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONAIR
Generic NameMASSAGER
Product CodeISA
Date Received2017-03-21
Model NumberBMS3
Device Availability*
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCONAIR CORPORATION
Manufacturer Address1 CUMMINGS POINT RD STAMFORD CT 06902 US 06902


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-03-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.