WHEELCHAIR ACCESSORY 2484686

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 2013-07-02 for WHEELCHAIR ACCESSORY 2484686 manufactured by H Fine & Son Ltd..

Event Text Entries

[63739779] Per importer's mdr: the dealer reported that the strap ripped off the sling which could cause the pt to fall.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004859134-2013-00006
MDR Report Key6210571
Report SourceDISTRIBUTOR
Date Received2013-07-02
Date of Report2013-07-02
Date Mfgr Received2013-06-29
Date Added to Maude2016-12-28
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 FDA3
Event Location3
Manufacturer ContactMR. KEVIN WALLS
Manufacturer Street33 GOLDEN EAGLE LN.
Manufacturer CityLITTLETON CO 80127
Manufacturer CountryUS
Manufacturer Postal80127
Manufacturer Phone7209625412
Manufacturer G1H FINE & SON LTD.
Manufacturer Street93 MANOR FARM RD.
Manufacturer CityWEMBLEY, MIDDLESEX HAO 1XB
Manufacturer CountryUP
Manufacturer Postal CodeHAO 1XB
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameWHEELCHAIR ACCESSORY
Generic NameSLING
Product CodeINE
Date Received2013-07-02
Model Number2484686
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerH FINE & SON LTD.
Manufacturer Address93 MANOR FARM RD. WEMBLEY, MIDDLESEX HAO 1XB UK HAO 1XB


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-07-02

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