CONAIR WW711

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-03 for CONAIR WW711 manufactured by Conair Corporation.

Event Text Entries

[129333829] On 12/3/2018 - the consumer discarded the product and agreed to a replacement. An investigation will not be performed do to the product being discarded.
Patient Sequence No: 1, Text Type: N, H10


[129333830] On (b)(6) 2018 - the consumer claims that glass on the unit shattered. No injuries occurred and the consumer agree to a replacement. The consumer discarded the product, therefore an investigation will not be completed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222304-2018-00027
MDR Report Key8126025
Date Received2018-12-03
Date of Report2018-11-05
Date of Event2018-11-04
Date Added to Maude2018-12-03
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,
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCONAIR
Generic NameBIA SCALES
Product CodeMNW
Date Received2018-12-03
Model NumberWW711
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCONAIR CORPORATION
Manufacturer Address1 CUMMINGS POINT RD STAMFORD 06902 US 06902


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-12-03

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