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

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    GETINGE

    FDA Adverse Event
    Malfunction ·GETINGE DISINFECTION AB·Product code MDZ·March 22, 2001

    O'BRIAN

    FDA Adverse Event
    Injury ·KNIGHT MEDICAL, INC.·Product code LZH·November 11, 1994

    O'BRIEN KMI KM 70

    FDA Adverse Event
    Malfunction ·KNIGHT MEDICAL INC·Product code LZH·May 1, 1997

    GENESIS II TIBIAL DRILL GUIDE, REF 71440238, SIZE 5, QTY: (1), NON-STERILE, Smith & Nephew, Inc., Memphis, TN 38116, USA Drill guide used as manual surgical instrument during knee replacement surgeries.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code LXH·April 20, 2010

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 11, 2018

    BINAXNOW RSV WAIVED 22T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GQG·March 21, 2024

    CARTO 3

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DQK·June 13, 2017

    THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·June 13, 2017

    TRUCLEAR

    FDA Adverse Event
    Injury ·MITG - OKLAHOMA CITY·Product code HIH·August 24, 2018

    PUMP MMT-1780KR 670G MG MEDI RECERT

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·August 3, 2023

    PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT-754DEP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 14, 2022

    MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 27, 2022

    MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 24, 2022

    PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT-754DEP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 8, 2022

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 1, 2024

    ION

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code EOQ·June 20, 2023

    RADIESSE INJECTABLE IMPLANT

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LMH·February 6, 2019

    MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 8, 2022

    Taut Intraducer Peritoneal Catheter, 12 Fr x 10 Fr x 20.3 cm; a sterile, Rx peritoneal catheter for single use, individually packaged in a Tyvek/clear pouch; Taut Inc., 2561 Kaneville Ct., Geneva, IL 60134; the individually packaged, sterilirzed catheter was sold in two configurations: a) catalog number (REF) P.I.-128: 10 catheters per box, 10 boxes per case, and b) a sterile component of the convenience kit, catalog number (REF) 50000, System One Comprehensive Lap CBDE Kit

    FDA Recall
    Terminated ·Taut, Inc.·Product code GBW·January 19, 2007