ACORN 180 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 2016-10-06 for ACORN 180 RH manufactured by Acorn Stairlifts, Inc..

Event Text Entries

[56936568] Seat appears to have broken at hinge. Component part manufacturer has investigated malfunction and determined low risk- see report 3006310491-2016-00002. Client would not release seat to acorn.
Patient Sequence No: 1, Text Type: N, H10


[56936569] Lift was parked at top of steps. Client went to sit on seat and it snapped off. No serious injuries.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003124453-2016-00006
MDR Report Key6002778
Report SourceCONSUMER
Date Received2016-10-06
Date of Report2016-10-06
Date of Event2016-09-06
Date Mfgr Received2016-09-07
Device Manufacturer Date2014-02-05
Date Added to Maude2016-10-06
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 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 180 RH
Generic NamePOWEREDSTAIRWAY CHAIRLIFT
Product CodePCD
Date Received2016-10-06
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerACORN STAIRLIFTS, INC.
Manufacturer Address7001 LAKE ELLENOR DRIVE ORLANDO FL 32809 US 32809


Patients

Patient NumberTreatmentOutcomeDate
10 2016-10-06

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