BEUDAMED
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    SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198

    FDA Recall
    Open, Classified ·WISSNER-BOSSERHOFF GMBH Hauptstr. 4-6 Wickede (Ruhr) Germany·Product code LLI·July 11, 2022

    MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L

    FDA Recall
    Open, Classified ·Product code LLI·November 26, 2025

    MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

    FDA Recall
    Open, Classified ·Product code LLI·November 26, 2025

    Hill-Rom brand TotalCare bed system; model P1900 -remanufactured only.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code LLI·March 15, 2004

    MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO

    FDA Recall
    Open, Classified ·Product code LLI·November 26, 2025

    Junction Box - 1104343 and 1193560

    FDA Recall
    Terminated ·Invacare Corporation·Product code LLI·December 2, 2016

    Bariatric Bed - BAR600IVC

    FDA Recall
    Terminated ·Invacare Corporation·Product code LLI·December 2, 2016

    Invacare IVC Home Care Bed (Foot Section with new head actuator from Linak.

    FDA Recall
    Terminated ·Invacare Corporation One Invacare Way·Product code LLI·June 9, 2003

    Craftmatic Model 1 Base for Dual Bed Configurations

    FDA Recall
    Open, Classified ·Craftmatic Industries, Inc.·Product code LLI·March 24, 2017

    MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.

    FDA Recall
    Open, Classified ·Product code LLI·November 26, 2025

    AC-powered Adjustable Hospital Bed. (ICCG Bed) Affected Model numbers: IH820-3MDLX, IHSC900DLX, IH820-3MDLX-QS, IH820-3MPDLX-QS, SC900-80WDLX-QSP, SC900-80PDLX-QSP, IH820-3MDLX-AE-333PS, SC90080GDLX-AE-366PA, SC90080GDLX-AE-333PS, IH820-3MDLX-AE-366PS, IH820-3MDLX-AE-333PA, IH820-3MDLX-AE-366PA and SC90080GDLX-AE-366PS

    FDA Recall
    Terminated ·Invacare Corporation·Product code LLI·September 27, 2006

    LUMEX A Graham-Field Brand, Bed End Sert. Low/Full-electric, Plastic Panels, Item 690-7604-000 Manufactured for : GF Heath Products, Inc., Atlanta, Georgia 30360 Made in China. LUMEX A Graham-Field Brand, Bed End Sert. Low/Full-electric, Walnut Panels, Item 690-7004-000 Manufactured for : GF Heath Products, Inc., Atlanta, Georgia 30360 Made in China. Therapeutic bed intended for home use.

    FDA Recall
    Terminated ·GF Health Products, Inc./d.b.a.Basic American Metal Products·Product code LLI·April 17, 2012

    Bariatric Bed - BARPKG-IVC 1633

    FDA Recall
    Terminated ·Invacare Corporation·Product code LLI·December 2, 2016

    Invacare 600 lb. Bariatric Bed, Head motor extension cable used on component numbers BAR5490 and BAR5490IVC. These components are part of the following Bed Model Number(s): BAR600, BARPKGCA, BAR600IVC, BARPKGIVC-1633, and BARPKG.

    FDA Recall
    Terminated ·Invacare Corporation·Product code LLI·June 23, 2011

    Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW

    FDA Recall
    Open, Classified ·Invacare Corporation·Product code LLI·January 22, 2024

    MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO

    FDA Recall
    Open, Classified ·Product code LLI·November 26, 2025

    Legacy Base for Dual Bed Configurations

    FDA Recall
    Open, Classified ·Craftmatic Industries, Inc.·Product code LLI·March 24, 2017

    Foot Section - BAR5490IVC

    FDA Recall
    Terminated ·Invacare Corporation·Product code LLI·December 2, 2016

    MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4

    FDA Recall
    Open, Classified ·Product code LLI·November 26, 2025

    1) Vascular Dilator, Sterile EO, Rx Only, Catalog #: DIL-100-12; 2) Dilator, Sterile EO, Rx Only, Catalog #: DIL-600-11; 3) Tearaway Introducer, Sterile EO, Rx Only, Catalog #: a) INT-028-14; b) INT-028-24; c) INT-029-05; d) INT-106-01; e) INT-106-14; 4) Micro-Access Tearaway Introducer Kit, Sterile EO, Rx Only, Catalog #: KIT-010-14; 5) Mini Tear Away Introducer Kit, Sterile EO, Rx Only, Catalog #: KIT-027-04; 6) LI-11 Plus G, Sterile EO, Catalog #: KIT-042-11; 7) LI-12 Plus G, Sterile EO, Catalog #: KIT-042-12; 8) Micro-Access Tearaway Introducer Kit, Sterile EO, Catalog #: a) KIT-900-13; b) KIT-900-14; c) KIT-900-17; d) KIT-900-29; e) KIT-901-02; f) KIT-901-02; 9) "Micro-Access" Kit, Sterile EO, Catolog #: KIT-900-88 10) Mini Stick II Microintroducer Kit. Sterile EO, Rx Only, Catalog #: a) KIT-045-05; b) KIT-045-15;

    FDA Recall
    Terminated ·Galt Medical Corporation·Product code DYB·May 2, 2018