• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: QUICKIE/MOTION CONCEPTS POWER WHEELCHAIR

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

QUICKIE/MOTION CONCEPTS POWER WHEELCHAIR Back to Search Results
Device Problem Mechanics Altered (2984)
Patient Problem Emotional Changes (1831)
Event Date 10/18/2015
Event Type  Injury  
Event Description
I recently ((b)(6) 2015) got a new power chair with a tilt feature for pressure release.On (b)(6), while in full tilt recline the chair would not release and return to an upright position.It was about 11 pm and my first action was to call the company that sold me the chair.I contacted a rep who tried to help to no avail.She had a tech call me and again the tech was not able to give me any advice as to how to resolve my issue.My wife and daughter were with me and luckily they were able to undo the wheel stop, bring me next to my bed and physically lift me out of the chair.This was not an easy process, my daughter is a physical therapist and at least had the knowledge to know how to lift me safely.If i had been alone or with just my wife i would have to, have called 911.This type of chair needs a manual, mechanical release in case of electronic/computer break downs.This chair could have caused me serious physical injury breaking down in the full tilt position.As it is i have had several nights of nightmares, as the hour or so that i was stuck in the chair was quite nerve wracking.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
POWER WHEELCHAIR
Type of Device
POWER WHEELCHAIR
Manufacturer (Section D)
QUICKIE/MOTION CONCEPTS
MDR Report Key5187441
MDR Text Key29941773
Report NumberMW5057503
Device Sequence Number1
Product Code ITI
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 10/26/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/26/2015
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age61 YR
Patient Weight100
-
-