POWER LIFT W/LOW BASE-PLUS 9153633519 NA:RPL450-1 RPL450-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-25 for POWER LIFT W/LOW BASE-PLUS 9153633519 NA:RPL450-1 RPL450-1 manufactured by Invamex Manufacturing.

MAUDE Entry Details

Report Number9616091-2020-00015
MDR Report Key9878182
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-25
Date of Report2020-02-26
Date Mfgr Received2020-02-26
Device Manufacturer Date2012-12-01
Date Added to Maude2020-03-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JASON FIEST
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44035
Manufacturer CountryUS
Manufacturer Postal44035
Manufacturer Phone8003336900
Manufacturer G1INVAMEX MANUFACTURING
Manufacturer Street102 PARQUE INDUSTRIAL MANIMEX
Manufacturer CityREYNOSA, TAMAULIPAS 88780
Manufacturer CountryMX
Manufacturer Postal Code88780
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePOWER LIFT W/LOW BASE-PLUS 9153633519
Generic NameLIFT, PATIENT, NON-AC-POWERED
Product CodeFSA
Date Received2020-03-25
Returned To Mfg2020-03-13
Model NumberNA:RPL450-1
Catalog NumberRPL450-1
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerINVAMEX MANUFACTURING
Manufacturer Address102 PARQUE INDUSTRIAL MANIMEX REYNOSA, TAMAULIPAS 88780 MX 88780


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.