CONAIR WW711F

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-01 for CONAIR WW711F manufactured by Conair Corporation.

Event Text Entries

[99094516] On 2/1/2018 - the consumer decided to return the product to our warehouse and accepted a replacement. No investigation is required.
Patient Sequence No: 1, Text Type: N, H10


[99094517] On 1/29/2017 - the consumer claims the glass has shattered on the product. No injuries occurred. The consumer accepted a replacement product.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222304-2018-00002
MDR Report Key7233703
Date Received2018-02-01
Date of Report2017-12-25
Date of Event2017-12-21
Date Added to Maude2018-02-01
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 Report0

Device Details

Brand NameCONAIR
Generic NameBMI SCALE
Product CodeMNW
Date Received2018-02-01
Model NumberWW711F
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 2018-02-01

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