BEUDAMED
    35 results · 12ms · Sources: EU EUDAMED, US FDA

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    Prisma continuous renal replacement system.

    FDA Recall
    Terminated ·Gambro Renal Products·Product code KDI·August 16, 2005

    Cidexplus Solution Test Strips

    FDA Recall
    Terminated ·Advanced Sterilization Products·Product code JOJ·March 16, 2005

    Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 8.0mm Product Number: 538080E

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·May 16, 2005

    Portex Per-Fit Percutaneous Dilational Tracheostomy Kit ,ID 7.0mm Product Number: 535070

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·May 16, 2005

    Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 9.0mm Product Number: 538090E

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·May 16, 2005

    Portex Per-Fit Percutaneous Dilational Tracheostomy Kit, ID 8.0mm Product Number: 535080

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·May 16, 2005

    Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 7.0mm Product Number: 538070E

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·May 16, 2005

    Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 9.0mm Product Number: 535090

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·May 16, 2005

    GEM PREMIER 3000

    FDA Recall
    Terminated ·Instrumentation Laboratory Co.·Product code CGA·December 16, 2005

    Sodium Chloride Injection USP, manufactured by IV Flush LLC

    FDA Recall
    Terminated ·IV Flush LLC·Product code FOZ·January 26, 2005

    Heparin Lock Flush Solution, manufactured by IV Flush LLC

    FDA Recall
    Terminated ·IV Flush LLC·Product code FOZ·January 26, 2005

    BD 25G Spinal Needles. (Spinal Anesthesia Needle)

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code BSP·March 16, 2005

    EBI Ball Tip Guide Wire 3.2mm x 55cm found in the Ankle Arthrodesis Nail Instr., Part Number 469055.

    FDA Recall
    Terminated ·Product code HXI·March 16, 2005

    PG910 Spacers, Part number SP101, loaded into Bard Express Seeding Cartridges containing TheraSeed Pd-103 devices. The product is shipped non-sterile in a foil pouch, packed 50 loose spacers per pouch.

    FDA Recall
    Terminated ·Theragenics Corporation·Product code KXK·May 16, 2005

    EBI Ball Tip Guide Wire 3.2mm x 98cm found in the Holland Nail Flexible Reamer Accessory P/N 469060.

    FDA Recall
    Terminated ·Product code HXI·March 16, 2005

    Threaded Tip GD Pin 1/8in x 9in Pk 5 Sterile found in Uniflex Profile Tibial Nail P/N 329640.

    FDA Recall
    Terminated ·Product code HXI·March 16, 2005

    CELL-DYN CD 3/4/8 Assay Reagents for Sapphire Hematology Analyzer

    FDA Recall
    Terminated ·Abbott Laboratories·Product code GKZ·December 16, 2005

    The TRIO Spondylolisthesis Reduction Instrument is a Class I Manual Surgical Instrument unique to the implantation of Stryker Spine TRIO PS this instrument is intended for use in the reduction of degenerative Spondylolisthesis.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code MNH·May 16, 2005

    Advisor Vital Signs Monitor (model 9200) with Capnography options installed (model 9212S or model 9212A), catalog no. 920654225.

    FDA Recall
    Terminated ·Smiths Medical PM, Inc.·Product code DPS·March 16, 2005

    Advisor Vital Signs Monitor (model 9200) with Capnography options installed (model 9212S or model 9212A), catalog no. 925574325.

    FDA Recall
    Terminated ·Smiths Medical PM, Inc.·Product code DPS·March 16, 2005