BEUDAMED
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    PRISMASATE DIALYSIS SOLUTION FOR CONTINUOUS RENAL REPLACEMENT THERAPY 5000ML BAG

    FDA Adverse Event
    Malfunction ·GAMBRO·Product code FII·December 2, 2009

    PRISMASATE BGK 4/2.5

    FDA Adverse Event
    Other ·GAMBRO RENAL PRODUCTS, INC.·Product code FJK·April 12, 2006

    PRISMASOL BGK 2/0

    FDA Adverse Event
    Malfunction ·GAMBRO/BAXTER·Product code KPO·March 22, 2017

    PRISMASOL BGK 4/2.5 CRRT BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KPO·May 26, 2021

    EXPANSE BLOOD BANK

    FDA Adverse Event
    Injury ·MEDICAL INFORMATION TECHNOLOGY, INC.·Product code MMH·December 18, 2025

    BD SYR MF 1CC 1S 28G

    FDA Adverse Event
    Malfunction ·BDK·Product code FMF·January 20, 2010

    FEMORAL LOCKING NAIL SMALL DIA., LEFT D11X400 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·April 13, 2005

    G/K FEMORAL NAIL

    FDA Adverse Event
    STRYKER HOWMEDICA KIEL TRAUMA GMBH·Product code JDS·December 4, 2003

    AUDIO EFFECTS GENERATOR

    FDA Adverse Event
    Malfunction ·BGC ENTERPRISES, INC.·January 2, 1996

    BAK/CERVICAL (BAK/C)

    FDA Adverse Event
    Injury ·SULZER SPINE TECH·Product code MAX·July 21, 2003

    BAK/CERVICAL (BAK/C)

    FDA Adverse Event
    Injury ·SULZER SPINE TECH·Product code MAX·June 4, 2003

    BAK

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·July 28, 2009

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 14, 2019

    ULTRASOUND 2001 LEOPARD

    FDA Adverse Event
    Malfunction ·B.K. MEDICAL SYSTEMS, INC.·Product code ITX·June 10, 2010

    BAK/VISTA

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code MAX·June 9, 2010

    BAK IMPLANT

    FDA Adverse Event
    Other ·SPINE TECH INC.·Product code MAX·August 10, 2003

    BAK/L

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWP·November 12, 2009

    BAK/PROXIMITY

    FDA Adverse Event
    Injury ·CENTERPULSE SPINE-TECH (SULZER-SPINETECH)·Product code MAX·March 7, 2003

    BAK INSTRUMENTATION

    FDA Adverse Event
    Injury ·SULZER SPINE-TECH·Product code LXH·August 3, 1998

    BAK INSTRUMENTATION

    FDA Adverse Event
    Injury ·SULZER SPINE-TECH·Product code LXH·August 13, 1998