ACORN 130 RH

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2017-01-13 for ACORN 130 RH manufactured by Acorn Stairlifts, Inc..

Event Text Entries

[64907206] Most likely underlying cause was either foreign object contacting/bridging leads on the back side of the power connections at pcb or power surge from outside the lift.
Patient Sequence No: 1, Text Type: N, H10


[64907207] Customer reported chemical smell; upon inspection, found hole in carriage cover and pcb burnt.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003124453-2017-00002
MDR Report Key6251312
Report SourceCOMPANY REPRESENTATIVE
Date Received2017-01-13
Date of Report2017-01-13
Date of Event2016-12-13
Date Mfgr Received2016-12-14
Device Manufacturer Date2016-12-08
Date Added to Maude2017-01-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT FAMILY MEMBER OR FRIEND
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. TRACY BERO
Manufacturer Street7001 LAKE ELLENOR DRIVE
Manufacturer CityORLANDO FL 32809
Manufacturer CountryUS
Manufacturer Postal32809
Manufacturer Phone4076500216
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACORN 130 RH
Generic NamePOWERED STAIRWAY CHAIRLIFT, PRODUCT CODE PCD
Product CodePCD
Date Received2017-01-13
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerACORN STAIRLIFTS, INC.
Manufacturer Address7001 LAKE ELLENOR DRIVE ORLANDO FL 32809 US 32809


Patients

Patient NumberTreatmentOutcomeDate
10 2017-01-13

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