INVACARE PROPEL BACK 16 IN WIDE PCPROPEL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2015-01-23 for INVACARE PROPEL BACK 16 IN WIDE PCPROPEL manufactured by Invacare Cleveland Street.

Event Text Entries

[5393885] It has been reported by a provider that over time, the bolts came loose on a propel back, and the bracket that attaches to the back of the seating broke off.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219590-2015-00026
MDR Report Key4448455
Report Source08
Date Received2015-01-23
Date of Report2015-01-16
Date Mfgr Received2015-01-16
Date Added to Maude2015-02-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactKEVIN GUYTON
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44036
Manufacturer CountryUS
Manufacturer Postal44036
Manufacturer Phone8003336900
Manufacturer G1INVACARE CLEVELAND STREET
Manufacturer Street899 CLEVELAND STREET
Manufacturer CityELYRIA OH 44036
Manufacturer CountryUS
Manufacturer Postal Code44036
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINVACARE PROPEL BACK 16 IN WIDE
Generic NameCUSHION, WHEELCHAIR
Product CodeKNN
Date Received2015-01-23
Model NumberPCPROPEL
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINVACARE CLEVELAND STREET
Manufacturer Address899 CLEVELAND STREET ELYRIA OH 44036 US 44036


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-01-23

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