BEUDAMED
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    MEDRAD® Stellant Sterile Disposable Syringe

    FDA UDI
    BAYER MEDICAL CARE INC.·00616258009896·KIT,SYR,STLNT,SJS-PT-J,MC,JA2 (85231499)

    PT²¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (HEREDIA)·Product code DQX·May 17, 2018

    ATTUNE DISTAL FEMORAL JIG

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND 9616671·Product code HWT·August 21, 2018

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NIQ·July 6, 2004

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NIQ·July 6, 2004

    STELLANT CT SYRINGE KIT

    FDA Adverse Event
    Malfunction ·BAYER MEDICAL CARE, INC.·Product code DXT·November 16, 2017

    GUIDE WIRES

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQX·October 20, 2004

    GUIDE WIRES

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQX·October 20, 2004

    STELLANT CT SYRINGE KIT

    FDA Adverse Event
    Malfunction ·BAYER MEDICAL CARE, INC.·Product code DXT·August 4, 2014

    OPTETRAK HI-FLEX TIBIAL INSERT SZ 4 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2025

    PT²¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DQX·October 5, 2012

    STELLANT DUAL CT INJECTOR

    FDA Adverse Event
    Injury ·BAYER MEDICAL CARE INC.·Product code DXT·October 23, 2023

    Scimed ChoICE PT ''J'' Tip 182 cm Guide Wire, a single use, sterile (EO), device packaged in a carrier tube, which is held in a coil by plastic clips. The carrier tube assembly of the guide wire is sealed into a pouch. The pouch assembies are packaged in a five-pack product box.

    FDA Recall
    Terminated ·Symbiosis Corp.·Product code DQX·July 16, 2002

    CHOICE (TM)

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DQX·March 28, 2012

    MAVERICK BALLOON DILATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·March 28, 2012

    TRAPEZOID TIBIAL TRAY SZ 4F/3T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2025

    OPTETRAK ASY, HI-FLEX PS CEM FEM, SZ 4, RIGHT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2025

    RAPIDEC CARBA NP

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, SA·Product code PTJ·September 2, 2020

    RAPIDEC CARBA NP

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code PTJ·November 25, 2020

    RAPIDEC® CARBA NP (10) US

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code PTJ·October 12, 2021