BEUDAMED
    47 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Recall × Status: Terminated × Clear all

    AUTO REF/KERATOMETER ARK-1s

    FDA Recall
    Terminated ·Nidek Inc.·Product code HKO·December 20, 2017

    Insert for IRK for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    IRK QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System and Si-e. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Vision Troubleshooting Guide for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Vessel Sealer QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Single Site US Manuals and Single Site OUS Manuals for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Stapler Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Cautery QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Endowrist Instrument and Accessory Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Connection QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Vessel Sealer Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    Natural Rubber Latex QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    System Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

    FDA Recall
    Terminated ·Intuitive Surgical, Inc.·Product code NAY·May 21, 2014

    0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.

    FDA Recall
    Terminated ·MRP, LLC dba AMUSA·Product code NGT·April 27, 2015

    Weber SolarJet S CO2 Vector Laser Coder System; Weber Marking Systems, Inc., Arlington Heights, IL 60005

    FDA Recall
    Terminated ·Weber Marking System Inc.·Product code LS-99·September 12, 2003

    0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.

    FDA Recall
    Terminated ·MRP, LLC dba AMUSA·Product code NGT·July 2, 2015

    T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe.

    FDA Recall
    Terminated ·MRP, LLC dba AMUSA·Product code NGT·February 9, 2015

    Welch Allyn PIC 50 Portable Intensive Care System Multi-Parameter Monitor/Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois 60089

    FDA Recall
    Terminated ·MRL, Inc., A Welch Allyn Company·Product code MJK·June 30, 2006

    Welch Allyn PIC 50 Portable Intensive Care System, Multi-Parameter Monitor/Defibrillator; a portable 12V internal battery powered defibrillator; Manufactured by MRL Inc., a WelchAllyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois 60089-Part Numbers-971081,971082,971083,971084.

    FDA Recall
    Terminated ·MRL, Inc., A Welch Allyn Company·Product code MJK·November 15, 2006

    Welch Allyn AED 10 Defibrillator; a battery powered automated external defibrillator; Manufacturer: MRL, Inc., A Welch Allyn Company, 100 Asbury Drive, Buffalo Grove, Illinois 60089; Model AED10, part numbers 970300 (defibrillator) and 970302 (defibrillator with soft shell carrying case)

    FDA Recall
    Terminated ·MRL, Inc., A Welch Allyn Company·Product code MKJ--·April 26, 2004