GENERIC 180 T565 LH US

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 2020-02-03 for GENERIC 180 T565 LH US manufactured by Acorn Stairlifts, Inc..

MAUDE Entry Details

Report Number3003124453-2020-00003
MDR Report Key9662578
Report SourceCONSUMER
Date Received2020-02-03
Date of Report2020-03-19
Date of Event2019-12-08
Date Mfgr Received2020-01-04
Device Manufacturer Date2019-03-18
Date Added to Maude2020-02-03
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. DORIAN PEARSON-SHAVER
Manufacturer Street7001 LAKE ELLENOR
Manufacturer CityORLANDO, FL FL 32809
Manufacturer CountryUS
Manufacturer Postal32809
Manufacturer Phone4076500216
Manufacturer G1ACORN STAIRLIFTS, INC.
Manufacturer Street7001 LAKE ELLENOR DRIVE
Manufacturer CityORLANDO, FL FL 32809
Manufacturer CountryUS
Manufacturer Postal Code32809
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGENERIC 180 T565 LH US
Generic NamePOWER STAIRWAY CHAIR LIFT
Product CodePCD
Date Received2020-02-03
Returned To Mfg2020-01-31
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerACORN STAIRLIFTS, INC.
Manufacturer Address7001 LAKE ELLENOR DRIVE ORLANDO, FL FL 32809 US 32809


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-02-03

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