59 T EZ GLIDE CHAIR 0731328

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-10 for 59 T EZ GLIDE CHAIR 0731328 manufactured by Ferno-washington, Inc..

Event Text Entries

[130179897] It was reported while transporting a patient the seat frame of the chair allegedly broke. The patient was properly restrained and no injuries occured; however, the patient was transferred to an alternate method to continue the transport.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1523574-2018-00041
MDR Report Key8147294
Date Received2018-12-10
Date of Report2019-02-04
Date of Event2018-11-17
Date Mfgr Received2018-12-05
Device Manufacturer Date2006-06-01
Date Added to Maude2018-12-10
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 ContactMS. DAWN GREENE
Manufacturer Street70 WEIL WAY
Manufacturer CityWILMINGTON OH 45177
Manufacturer CountryUS
Manufacturer Postal45177
Manufacturer Phone9372832900
Manufacturer G1FERNO-WASHINGTON, INC.
Manufacturer Street70 WEIL WAY
Manufacturer CityWILMINGTON OH 45177
Manufacturer CountryUS
Manufacturer Postal Code45177
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand Name59 T EZ GLIDE CHAIR
Generic Name59 T EZ GLIDE CHAIR
Product CodeFPP
Date Received2018-12-10
Model Number0731328
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerFERNO-WASHINGTON, INC.
Manufacturer Address70 WEIL WAY WILMINGTON OH 45177 US 45177


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-10

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