PRIDE MOBILITY PRODUCTS IDT100-1 N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-10-18 for PRIDE MOBILITY PRODUCTS IDT100-1 N/A manufactured by Pride Mobility Products.

Event Text Entries

[124161871] The device has not been made available for evaluation at this time. Should the device or more information become available, a follow-up report will then be issued.
Patient Sequence No: 1, Text Type: N, H10


[124161872] Alleges the forward drive sensor is not activating properly and the chair would not stop causing injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2530130-2018-00148
MDR Report Key7979742
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-10-18
Date of Report2018-11-20
Date Mfgr Received2018-09-25
Date Added to Maude2018-10-18
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 ContactMISS KELLY LIVINGSTON
Manufacturer Street401 YORK AVE N/A
Manufacturer CityDURYEA PA 18642
Manufacturer CountryUS
Manufacturer Postal18642
Manufacturer Phone5706555574
Manufacturer G1N/A
Manufacturer StreetN/A N/A
Manufacturer CityN/A
Manufacturer CountryUS
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NamePRIDE MOBILITY PRODUCTS
Generic NameWHEELCHAIR COMPONENT
Product CodeKNN
Date Received2018-10-18
Returned To Mfg2018-11-15
Model NumberIDT100-1
Catalog NumberN/A
Lot NumberN/A
OperatorLAY USER/PATIENT
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerPRIDE MOBILITY PRODUCTS
Manufacturer Address401 YORK AVE N/A DURYEA PA 18642 US 18642


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-10-18

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