WILLOW WEARABLE BREAST PUMP PDW29

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 2020-03-26 for WILLOW WEARABLE BREAST PUMP PDW29 manufactured by Exploramed Nc7, Inc..

MAUDE Entry Details

Report Number3012759464-2020-00002
MDR Report Key9887172
Report SourceCONSUMER
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2020-03-04
Date Mfgr Received2020-03-12
Device Manufacturer Date2019-12-27
Date Added to Maude2020-03-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMR. NELSON LAM
Manufacturer Street1975 W. EL CAMINO REAL SUITE 306
Manufacturer CityMOUNTAIN VIEW, CA
Manufacturer CountryUS
Manufacturer Phone9898681
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameWILLOW WEARABLE BREAST PUMP
Generic NamePOWERED BREAST PUMP
Product CodeHGX
Date Received2020-03-26
Model NumberPDW29
Catalog NumberPDW29
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerEXPLORAMED NC7, INC.
Manufacturer Address1975 W. EL CAMINO REAL SUITE 306 MOUNTAIN VIEW, CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-26

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