DAILY ACTIVITY ASSIST DEVICES 6365

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2014-05-30 for DAILY ACTIVITY ASSIST DEVICES 6365 manufactured by Invacare Cleveland Street.

Event Text Entries

[17263388] Dealer stated that the seat on a 6365 commode has cracked. .
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219590-2014-00086
MDR Report Key3841462
Report Source08
Date Received2014-05-30
Date of Report2014-04-14
Date Mfgr Received2014-04-14
Date Added to Maude2014-07-02
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 FDA0
Event Location0
Manufacturer ContactGREGORY STEVENS
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 NameDAILY ACTIVITY ASSIST DEVICES
Generic Name890.5050
Product CodeINB
Date Received2014-05-30
Model Number6365
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
101. Other 2014-05-30

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