BEUDAMED
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    Gold Lion Water-Base 8oz

    FDA UDI
    JAD PARTNERS CORP.·00860015384416·Water-Based Personal Lubricant

    Gold Lion Water-Base 4oz

    FDA UDI
    JAD PARTNERS CORP.·00860015384409·Water-Based Personal Lubricant

    VAIL PRODUCTS

    FDA Adverse Event
    Other ·VAIL PRODUCTS·Product code FNJ·March 5, 2005

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 12, 2025

    TRIDENT 0 X3 INSERT 23 MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS - MAHWAH·Product code LPH·October 19, 2011

    CS100 INTRA-AORTIC BALLOON PUMP, CHINESE, 220V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 23, 2023

    CONTINUOUS EPIDURAL

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code CAZ·March 20, 2001

    ENDOVIVE STANDARD BALLOON REPLACEMENT KIT, 20 FR

    FDA Adverse Event
    Injury ·XERIDIEM MEDICAL DEVICES·Product code KNT·June 5, 2017

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 15, 2011

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·March 17, 2021

    ONE TOUCH ULTRA

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code CFR·April 5, 2005

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·June 10, 2025

    UNKNOWN STRATA VALVE/SHUNT

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·December 20, 2018

    BLADE/SCREW GUIDE SLEEVE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code FZX·October 29, 2019

    JADA SYSTEM

    FDA Adverse Event
    Malfunction ·ALYDIA HEALTH·Product code OQY·April 29, 2022

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 2, 2018

    HEMOSPRAY ENDOSCOPIC HEMOSTAT

    FDA Adverse Event
    Injury ·WILSON-COOK MEDICAL INC·Product code QAU·February 13, 2026

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·June 13, 2018

    DERMOPAN-1 SYSTEM

    FDA Adverse Event
    Injury ·SIEMENS MED SOLUTIONS USA, INC.·Product code JAD·March 9, 2012

    XOFT AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·XOFT, A SUBSIDIARY OF ICAD, INC.·Product code JAD·May 14, 2014