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584 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen

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  1. Becton, Dickinson and Company, IDS-23-4859, BD BACTEC™ Plus Aerobic/F Culture Vials

    BD heeft via twee klachten van klanten bevestigd dat bepaalde flesjes van de hierboven vermelde BD BACTEC™ Plus ...

    Waarschuwing | 21-09-2023

  2. Beckman Coulter, Inc., FA 23026, Access Folate (Reagent Pack)

    Beckman Coulter heeft vastgesteld dat de reagenspipetten voor de DxI 9000 Access-immunoassay-analyser mogelijk niet volledig door ...

    Waarschuwing | 21-08-2023

  3. MED TRUST Handelsges.m.b.H., FSN-2023-01, Wellion LUNA TEST STRIPS 10 GLU

    Re·call Wellion LUNA duo/trio meter sets and teststrips. During an unannounced audit by TUV Rheinland it was detected that the ...

    Waarschuwing | 04-05-2023

  4. Biohit Oyj, 144-22, BIOHIT ColonView quick test

    lf the specified kit lot has been used, a minor possibility for a false negative result still exists. In such a case there would ...

    Waarschuwing | 30-12-2022

  5. Abbott Hematology, FA09SEP2022, Alinity hq Analyzer and Alinity hs Slide Maker Stainer Module

    The Alinity h-series System Control Center (SCC) Application Software Version 4.3 (and below) and the Local User Interface (LUI) ...

    Waarschuwing | 27-09-2022

  6. Helena Biosciences NC476 - SAS Free Kappa_Lambda IEF Kit

    Further to customer feedback regarding the performance of the SAS Free Kappa IEF Kit: REF 102208 and SAS Free Lambda IEF Kit: REF ...

    Waarschuwing | 20-04-2022

  7. Abbott GmbH FA24MAR2022 - Alinity i Homocysteine Reagent Kit

    Abbott has identified that some reagent kits produce suboptimal calibrations resulting in a downward shift of quality control ...

    Waarschuwing | 19-04-2022

  8. IQ Products BV, FSN-FSCA-2020-01- INC323, FMH QuikQuant

    IQ Products BV meldt Filed Safety over FMH QuikQuant.

    Waarschuwing | 26-11-2020

  9. RAL Diagnostics, NC 19/077, NC 19/080 et NC 19/111- CE.101, Giemsa Solution

    Concerning Giemsa Solution lot I88021, lot I97523 and lot I63818 which have a staining defect, 3 cases may appear during the use ...

    Waarschuwing | 11-11-2019

  10. Scimedx 19-02 - Scimedx Toxocara kit

    This letter is to inform you that Scimedx Corporation initiated a recall to remove the following kit due to reduced sensitivity.

    Waarschuwing | 02-08-2019

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