SITZ BATH 1616700692 IH3800

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-06-03 for SITZ BATH 1616700692 IH3800 manufactured by Invacare Cleveland Street.

Event Text Entries

[46855533] Should additional information become available, a supplemental record will be filed.
Patient Sequence No: 1, Text Type: N, H10


[46855534] Customer states the door is leaking.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219590-2016-00098
MDR Report Key5697117
Date Received2016-06-03
Date of Report2016-05-13
Date Mfgr Received2016-05-13
Date Added to Maude2016-06-03
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 FLORIDA OPERATIONS
Manufacturer Street2101 EAST LAKE MARY BLVD
Manufacturer CitySANFORD FL 32773
Manufacturer CountryUS
Manufacturer Postal Code32773
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSITZ BATH 1616700692
Generic NameBATH, SITZ, NONPOWERED
Product CodeKTC
Date Received2016-06-03
Model NumberIH3800
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINVACARE CLEVELAND STREET
Manufacturer Address899 CLEVELAND STREET ELYRIA OH 44036 US 44036


Patients

Patient NumberTreatmentOutcomeDate
10 2016-06-03

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