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

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    Optima Poly Screw Driver.

    FDA Recall
    Terminated ·U & I America·Product code MNI·August 18, 2003

    Optima Large Poly Screw Driver

    FDA Recall
    Terminated ·U & I America·Product code MNI·August 18, 2003

    Rultract Surgical Retractor, 4100 Series, all system configurations, reusable.

    FDA Recall
    Terminated ·Rultract Inc·Product code DWS·September 18, 2003

    Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)

    FDA Recall
    Terminated ·I-Flow Corporation·March 18, 2003

    LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 12140, Lot FH041202 Size 4, Catalog No. 12150, Lot FJ021202

    FDA Recall
    Terminated ·LMA North America Inc·Product code CAE·June 18, 2003

    Bucky Diagnost FS Part number 9890-010-83651

    FDA Recall
    Terminated ·Philips Medical Systems Sales & Service Region No. America·Product code KPR·November 18, 2003

    Premier CMV IgG Elisa Kits, EIA diagnostic test kits, 96 tests per kit, Catalog Numbers: 620096 and 9Z9501G.

    FDA Recall
    Terminated ·Meridian Bioscience Inc·Product code LFZ·June 18, 2003

    Access Immunoassay System Technical Update 03.1, Part number 387851, Software version 3.29

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code KLS·June 18, 2003

    On-Site Alcohol IVD A single use enzymatic assay for qualitative detection of alcohol in urine or saliva. Catalog numbers: 47464 Roche Diagnostics Label A305-02 Varian, Inc. label

    FDA Recall
    Terminated ·Varian, Inc.·Product code DML·July 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 5 std. stem; part 164245

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 2 std. stem; part 164242

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 4 std. stem; part 164244

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 1 straight stem; part 164251

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 3 straight stem; part 164253

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 2 straight stem; part 164252

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 3 std. stem; part 164243

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 5 straight stem; part 164255

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 1 std. stem; part 164241

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    Stanmore modular hip system; Stanmore CoCr femoral size 4 straight stem; part 164254

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDI·June 18, 2003

    BIOMERIEUX, Thromboplastin Reagent, Simplastin Excel S, 6 ml Diluent, bioMerieux, Inc., Durham, NC 27704

    FDA Recall
    Terminated ·Biomerieux, Inc.·Product code GJS·December 23, 2002