ACORN 130 RH

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-04-05 for ACORN 130 RH manufactured by Acorn Stairlifts, Inc..

Event Text Entries

[71824650] Customer's grandson was helping him onto the stairlift at the top of the stairs. The stairlift was locked in a 45 degree angle. The grandson turned his back to move the customer's walker out of the way when the customer tried to slide himself back onto the chair. At that point, the customer fell over the armrest of the chair and down the stairs. The customer was taken to the hospital and suffered fractured ribs and a concussion. Stairlift was inspected and all components operated to spec.
Patient Sequence No: 1, Text Type: N, H10


[71824651] Customer was being assisted onto the stairlift by his grandson. The stairlift was locked in the 45 degree position at the top of the staircase. Customer's grandson turned away to move the walker, at that point, the customer attempted to slide back onto the chair and fell over the armrest of the stairlift and down the stairs.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003124453-2017-00005
MDR Report Key6461873
Report SourceCONSUMER
Date Received2017-04-05
Date of Report2017-04-05
Date of Event2017-03-04
Date Mfgr Received2017-03-06
Device Manufacturer Date2017-01-17
Date Added to Maude2017-04-05
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 ContactMS TRACY BERO
Manufacturer Street7001 LAKE ELLENOR
Manufacturer CityORLANDO FL 328095792
Manufacturer CountryUS
Manufacturer Postal328095792
Manufacturer Phone4076500216
Single Use3
Remedial ActionIN
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACORN 130 RH
Generic NamePOWERED STAIRWAY CHAIRLIFT
Product CodePCD
Date Received2017-04-05
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerACORN STAIRLIFTS, INC.
Manufacturer Address7001 LAKE ELLENOR DRIVE ORLANDO FL 328095792 US 328095792


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2017-04-05

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