BRUNO ELECTRA-RIDE II SRE-2700

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 2008-03-19 for BRUNO ELECTRA-RIDE II SRE-2700 manufactured by Bruno Independent Living Aids.

Event Text Entries

[2016926] Customer bc was riding stairlift when seat/armrest malfunctioned causing her to tip over and out of the seat and fall down the steps. Bc was hospitalized due to injuries.
Patient Sequence No: 1, Text Type: D, B5


[9165324] At the time of this writing, the insurance companies have been involved and there is no further info available to pass along.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2131358-2008-00013
MDR Report Key2136668
Report Source08
Date Received2008-03-19
Date of Report2008-02-19
Date Mfgr Received2008-02-19
Device Manufacturer Date2003-01-01
Date Added to Maude2011-06-27
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 FDA0
Event Location0
Manufacturer ContactTERRY ANDRUS
Manufacturer Street1780 EXECUTIVE DR P.O. BOX 84
Manufacturer CityOCONOMOWOC WI 53066
Manufacturer CountryUS
Manufacturer Postal53066
Manufacturer Phone2625674990
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBRUNO ELECTRA-RIDE II
Generic NameINCLINED STAIRWAY ELEVATOR
Product CodeILK
Date Received2008-03-19
Model NumberSRE-2700
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBRUNO INDEPENDENT LIVING AIDS
Manufacturer AddressOCONOMOWOC WI US


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2008-03-19

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