BMI SCALE WW585

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 2016-05-04 for BMI SCALE WW585 manufactured by Conair Corporation.

Event Text Entries

[44390558] (b)(4) 2016 - we have requested the product be returned to the manufacturer for evaluation. To date, we have not received the device. Device not returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10


[44390559] (b)(6) 2016 - the consumer alleges that the product exploded into pieces of glass. The glass was embedded into the consumer's hand. It has not been determined if medical attention was received.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222304-2016-00025
MDR Report Key5630937
Report SourceCONSUMER
Date Received2016-05-04
Date of Report2016-04-04
Date of Event2016-03-23
Date Added to Maude2016-05-04
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 NameBMI SCALE
Generic NameBMI SCALE
Product CodeMNW
Date Received2016-05-04
Model NumberWW585
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 2016-05-04

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