WATERPIK SINUSENSE WATER PULSATOR SWI-615

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 2018-06-29 for WATERPIK SINUSENSE WATER PULSATOR SWI-615 manufactured by Water Pik, Inc..

Event Text Entries

[112786941] Not possible to verify the customer irritation and blistering.
Patient Sequence No: 1, Text Type: N, H10


[112786942] Per the customer.... Claims moisture entered the battery compartment. Customer attempted to remove the moisture from the battery compartment by blowing into the compartment. Customer claims back-splash of water landed on his face and caused irritation and blistering. Customer did not seek medical attention but claims he needed medication to return to work.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001712259-2018-00004
MDR Report Key7651842
Report SourceCONSUMER
Date Received2018-06-29
Date of Report2018-06-29
Date of Event2018-06-04
Date Mfgr Received2018-06-04
Device Manufacturer Date2012-10-01
Date Added to Maude2018-06-29
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 ContactMR. ROBERT VANDER VLIET
Manufacturer Street1730 EAST PROSPECT ROAD
Manufacturer CityFORT COLLINS CO 805530001
Manufacturer CountryUS
Manufacturer Postal805530001
Manufacturer Phone9702217063
Manufacturer G1WATER PIK, INC.
Manufacturer Street1730 EAST PROSPECT ROAD
Manufacturer CityFORT COLLINS CO 805530001
Manufacturer CountryUS
Manufacturer Postal Code805530001
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameWATERPIK SINUSENSE WATER PULSATOR
Generic NameORAL IRRIGATOR
Product CodeEFS
Date Received2018-06-29
Returned To Mfg2018-06-18
Model NumberSWI-615
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerWATER PIK, INC.
Manufacturer Address1730 EAST PROSPECT ROAD FORT COLLINS CO 805530001 US 805530001


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-06-29

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