BEUDAMED
    25 results · 12ms · Sources: EU EUDAMED, US FDA

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    Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Aortic Perfusion Cannula with plastic tip, 22 Fr. x 23 cm, Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Duraflo Treated Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm, Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Duraflo Treated Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm., Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm., Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm. , Edwards Lifesciences

    FDA Recall
    Terminated ·Edwards Lifesciences Research Medical, Inc.·Product code DWF·April 18, 2006

    Staclot LA 20 tests, Catalog #0594, LA Assay, Hexagonal Phase Phospholipid Neutralization Assay.

    FDA Recall
    Terminated ·Diagnostica Stago, Inc.·Product code GFO·July 18, 2006

    BacT/ALERT Classic System Software, Blood Culturing System

    FDA Recall
    Terminated ·bioMerieux, Inc.·Product code MDB·August 14, 2006

    BacT/ALERT 3D System Software, Blood Culturing System

    FDA Recall
    Terminated ·bioMerieux, Inc.·Product code MDB·August 14, 2006

    Genesis II, Cruciate Retaining, Oxinium, Femoral component, Size 5 right, Part No. 71420152

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code HSX·April 12, 2006

    Genesis II, Cruciate Retaining, Oxinium, Femoral component, Size 5 left, Part No. 71420136

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code HSX·April 12, 2006

    BacT/ALERT 3D 60 Systems Software, Blood Culturing System

    FDA Recall
    Terminated ·bioMerieux, Inc.·Product code MDB·August 14, 2006

    BacT/ALERT 3D Combo Systems Software, Blood Culturing System

    FDA Recall
    Terminated ·bioMerieux, Inc.·Product code MDB·August 14, 2006

    Kimberly-Clark/Ballard medical R2 triangle shaped non-radiolucent multifunction electrode products for adults.

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code MKJ·May 18, 2006

    Abbott brand CELL-DYN 22 Calibrator, a whole blood calibrator used to calibrate CELL-DYN hematology systems. Model numbers: 99120-01

    FDA Recall
    Terminated ·Abbott Laboratories·Product code KRY·September 18, 2006

    Kimberly-Clark/Ballard medical R2 triangle shaped non-radiolucent multifunction electrode products for pediatrics.

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code MKJ·May 18, 2006

    bioMerieux BacT/ALERT SN Anaerobic Culture Bottle-REF 259790

    FDA Recall
    Terminated ·bioMerieux, Inc.·Product code MDB·August 17, 2006

    Shelhigh No-React Pulmonic Valve Conduit. **'Shelhigh No-React, Pulmonic Valve Conduit, NR4000-PA-C'** **'Shelhigh, Inc., 650 Liberty Ave., Union, NJ 07083 USA'** **'Shelhigh Porcine Pulmonic Valve Conduit Prosthesis Model NR-4000 Series with 'No-React' treatment*, INSTRUCTIONS FOR USE'**.

    FDA Recall
    Terminated ·Shelhigh, Inc.·Product code MWH·January 18, 2006

    Rocker Reducer, part of the SiLo Spinal System, REF 8880014, Rx only, Material: Stainless Steel, qty: 1 ea, non-sterile, Medtronic Sofamor Danek, 1800 Pyramid Place Memphis, TN 38132, USA, Manufactured at: Bartlett, Tennessee, USA

    FDA Recall
    Terminated ·Medtronic Sofamor Danek Instrument Manufacturing·Product code MNI·December 18, 2006