SITZ BATH 1616700692 IH3800

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2016-06-08 for SITZ BATH 1616700692 IH3800 manufactured by Invacare Cleveland Street.

Event Text Entries

[46856346] A follow up will be sent if the product or additional information is obtained.
Patient Sequence No: 1, Text Type: N, H10


[46856347] The door seal was leaking.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219590-2016-00103
MDR Report Key5705804
Report SourceDISTRIBUTOR
Date Received2016-06-08
Date of Report2016-05-18
Date Mfgr Received2016-05-18
Date Added to Maude2016-06-08
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 CLEVELAND STREET
Manufacturer Street899 CLEVELAND STREET
Manufacturer CityELYRIA OH 44036
Manufacturer CountryUS
Manufacturer Postal Code44036
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSITZ BATH 1616700692
Generic NameBATH, SITZ, NONPOWERED
Product CodeKTC
Date Received2016-06-08
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 2016-06-08

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