BEUDAMED
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    Quickie brand Freestyle M11 & F11, C. G. Tilt, Powered Wheelchair; Product is manufactured and distributed by Sunrise Medical, 2842 Business Park Ave., Fresno, CA 93727

    FDA Recall
    Terminated ·Sunrise Medical Inc·Product code ITI·November 15, 2005

    Pronto Series Power Wheelchair, model M51.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·May 2, 2005

    Pronto M51 Wheelchair, component- seat

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·June 14, 2006

    Jazzy Select 6 with XLR Port Harness

    FDA Recall
    Terminated ·Pride Mobility Products Corp·Product code ITI·February 1, 2010

    Storm Series Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width configurations with power recline seating system and a conventional style back.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·January 15, 2015

    Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C

    FDA Recall
    Open, Classified ·Invacare Corporation·Product code ITI·November 12, 2021

    Power Wheelchair

    FDA Recall
    Open, Classified ·Merits Holdings Co. dba Merits Health Products, Inc.·Product code ITI·April 1, 2021

    Dunlee DA 200 Ultra & MX 200 Ultra CT X-Ray Tube Housing Assembly (989600088701); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR

    FDA Recall
    Terminated ·Permobil, Ab Arvaltsvagen 10·Product code ITI·September 1, 2017

    Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, TDXSP2X-MCG, TDXSP2V, TDXSP2V-HD, TDXSP2HD, TDXSP2HD-CG, TDXSP2HD-MCG

    FDA Recall
    Open, Classified ·Invacare Corporation·Product code ITI·November 12, 2021

    Invacare 2G Tarsys Seating System, Model 2GR.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·December 15, 2003

    Quickie Groove Power Wheelchair with QC (non-expandable) electronics, Model number EIPW13.

    FDA Recall
    Terminated ·Sunrise Medical Inc·Product code ITI·January 11, 2008

    Dunlee DA 200 PRO & MX 200 PRO CT X-Ray Tube Housing Assembly (989600088401); replacement x-ray tube housing assemblies; Dunlee, 555 North Commerce Street, Aurora, Illinois 60504 U.S.A.; part number 875-01

    FDA Recall
    Terminated ·Dunlee·Product code ITY·April 7, 2005

    Pronto Series Power Wheelchair, model M61.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·May 2, 2005

    Invacare Pronto Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio, 44035-4190, (800) 333 -6900.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·February 2, 2015

    Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is controlled by Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966).

    FDA Recall
    Terminated ·Sunrise Medical (US) LLC·Product code ITI·February 13, 2020

    UltraLite Vehicles powered by Rascal Motorized Vehicles.

    FDA Recall
    Terminated ·Electric Mobility Corp·Product code ITI·May 5, 2005

    Q-Logic Controller Software used on the following power wheelchairs: Q6000, Q6000XL, Q6000Z, R4000, Q600, Q600XL, Q610, Q1107, Q600E, and Dynamo 1107

    FDA Recall
    Terminated ·Pride Mobility Products Corp·Product code ITI·April 11, 2008

    Sunrise Medical Quickie Groove Power Wheelchair with Transit option The product is a powered wheelchair for human use.

    FDA Recall
    Terminated ·Sunrise Medical Inc·Product code ITI·November 13, 2006

    Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500

    FDA Recall
    Terminated ·Permobil, Ab Arvaltsvagen 10·Product code ITI·September 1, 2017