BEUDAMED
    1,070 results · 19ms · Sources: EU EUDAMED, US FDA

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    Terumo Advanced Perfusion System 1; 220V -240V; Model 801764 (sold outside of the U.S. only).

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code DTQ·November 10, 2006

    Terumo Advanced Perfusion System 1; 100V -120V, 15 A (circuit breaker), 50/60 Hz (20A power source required); Model 801763.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code DTQ·November 10, 2006

    Celesteion PCA-9000A/2 PET/CT System

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code KPS·May 8, 2015

    Toshiba Aquilion CT System TSX-301A

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 8, 2015

    Toshiba Aquilion CT System TSX-301C

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 8, 2015

    Toshiba Aquilion CT System TSX-301B

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 8, 2015

    Toshiba Aquilion CT System TSX-302A

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 8, 2015

    Toshiba Aquilion CT System TSX-303A

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 8, 2015

    Toshiba Aquilion CT System TSX-101A

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 8, 2015

    GEM FLOW COUPLER Monitor, PN 5156-00000-011

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code DPW·June 19, 2023

    Atellica CH Revised C Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223.

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code DCN·March 11, 2025

    BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation.

    FDA Recall
    Terminated ·Stryker Sustainability Solutions·Product code NLH·December 17, 2018

    2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute and chronic dialysis therapy in a healthcare facility Models: (1) 190713 2008T HEMODIALYSIS SYS., with CDX; (2) 190766 2008T HEMODIALYSIS SYSTEM W/BIBAG W/CDX ; (3) 191124 2008T HD SYS. CDX BLUESTAR; (4) 191126 2008T HD SYS. CDX W/BIBAG BLUESTAR

    FDA Recall
    Open, Classified ·Fresenius Medical Care Holdings, Inc.·Product code KDI·July 27, 2022

    EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

    FDA Recall
    Completed ·Philips Ultrasound Inc·Product code IYN·July 22, 2021

    Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613327464818, Sterile R, RX Only CE 0197

    FDA Recall
    Terminated ·Stryker Corporation·Product code MBI·July 19, 2019

    Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R, RX Only CE 0197

    FDA Recall
    Terminated ·Stryker Corporation·Product code MBI·July 19, 2019

    REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile

    FDA Recall
    Open, Classified ·Stryker Sustainability Solutions·Product code JOW·April 14, 2023

    Stryker Sustainability Solutions REF HARH36 Ethicon Endo-Surgery, Inc. Harmonic ACE +7, Shears with Advanced Hemostasis 5mm Diameter x 36cm - Product Usage: indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. The instruments can be used as an adjunct to or substitute for electrosurgery, lasers and steel scalpels in general, plastic, pediatric, gynecologic, urologic, thoracic, exposure to orthopedic structures (such as spine and joint space), sealing and transection of lymphatic vessels, and other open and endoscopic procedures.

    FDA Recall
    Open, Classified ·Stryker Sustainability Solutions·Product code NLQ·January 19, 2021

    REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder

    FDA Recall
    Terminated ·Stryker Sustainability Solutions·Product code KCY·January 21, 2022

    PrisMax System, Product Code 955724

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code KDI·March 15, 2022