BRAUN L917IB LIFT *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-02-07 for BRAUN L917IB LIFT * manufactured by Braun Corporation.

Event Text Entries

[288117] The facility is working with braun corp to repair, replace and address the product problem. In 2003, staff was lifting a wheelchair client up, using a braun l917ib lift. The lift worked as designed coming up to the correct position. As the operator began to pull the person off the lift into the bus, the lift began to stow. The lift pulled completely into the vertical stow position without any operation of the switches. The vehicle pump continued to run for approximately two minutes before it shut off. Fortunately, the operator was able to pull the person away from the lift quickly with no one receiving any injuries. They took this lift out of service and notified their lift dealer and service representative. The service mechanic was able to reproduce the condition and confirmed a defective solenoid in the pump housing. Fortunately the 50lbs switch was working, preventing the person from catapulting into the vehicle. The concerns are obvious. The potential injuries that could have occurred in this case, as well as the countless lift cycles their agency performs each day could be devastating. The agency currently uses 22 ada para-transit vehicles that serves approximately 75 wheelchair bound clients. All of these vehicles are equipped with braun ada lifts. Agency began using braun lifts in 1995 after considerable political pressure from a major competitor. They have since replaced all lifts from other manufacturers with braun products. The major reasons they switched over to braun lifts were the safety design features that were more suited to needs. The braun corporation also appeared to respond much better to design problems experienced in the field by customers such as them.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1027456
MDR Report Key441922
Date Received2003-02-07
Date of Report2003-02-07
Date of Event2003-01-14
Date Added to Maude2003-02-12
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameBRAUN
Generic NameWHEELCHAIR LIFT
Product CodeING
Date Received2003-02-07
Model NumberL917IB LIFT
Catalog Number*
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device Availability*
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key430897
ManufacturerBRAUN CORPORATION
Manufacturer AddressPO BOX 1654 SOUTH BEND IN 46634 US


Patients

Patient NumberTreatmentOutcomeDate
10 2003-02-07

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