SITZ BATH 1616700692 IH3602GXL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-02-10 for SITZ BATH 1616700692 IH3602GXL manufactured by Invacare Taylor Street.

Event Text Entries

[38409698] Should additional information become available for the patient a supplemental record will be filed.
Patient Sequence No: 1, Text Type: N, H10


[38409699] Per dealer, the tub seal was no longer keeping the water in and was leaking.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1525712-2016-00416
MDR Report Key5427813
Date Received2016-02-10
Date of Report2016-01-22
Date of Event2016-01-08
Date Mfgr Received2016-01-22
Date Added to Maude2016-02-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKEVIN GUYTON
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44035
Manufacturer CountryUS
Manufacturer Postal44035
Manufacturer Phone8003336900
Manufacturer G1INVACARE TAYLOR STREET
Manufacturer Street1200 TAYLOR STREET
Manufacturer CityELYRIA OH 44036
Manufacturer CountryUS
Manufacturer Postal Code44036
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSITZ BATH 1616700692
Generic NameBATH, SITZ, NONPOWERED
Product CodeILM
Date Received2016-02-10
Model NumberIH3602GXL
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINVACARE TAYLOR STREET
Manufacturer Address1200 TAYLOR STREET ELYRIA OH 44036 US 44036


Patients

Patient NumberTreatmentOutcomeDate
10 2016-02-10

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