Events

translation missing: fr.activerecord.attributes.event.titles.recall_field_safety_notice

Selon Saudi Food & Drug Authority, ce/cet/cette translation missing: fr.activerecord.attributes.event.types.recall_field_safety_notice concerne un dispositif en/au/aux/à Saudi Arabia qui a été fabriqué par Radiometer Medical.

Qu'est-ce que c'est?

Les avis de sécurité sont des communications que les fabricants de dispositifs médicaux ou leurs représentants font parvenir en particulier aux travailleurs du secteur médical, mais aussi aux utilisateurs de ces dispositifs. Les avis de sécurité concernent les actions entreprises quant aux dispositifs présents sur le marché et peuvent inclure des rappels et des alertes.

En savoir plus sur les données ici
  • Type d'événement
    Recall / Field Safety Notice
  • ID de l'événement
    mdprc 040 11 12 001
  • Date de mise en oeuvre de l'événement
    2014-01-30
  • Pays de l'événement
    Saudi Arabia
  • Source de l'événement
    SFDA
  • URL de la source de l'événement
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=4&rid=5208
  • Notes / Alertes
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug Authority, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Saudi Arabia.
  • Notes supplémentaires dans les données
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Cause
    Radiometer recently became aware that some membranes may have enzyme residues on the outer membrane. upon replacement of the lactate membrane the enzyme residue may cause an initial negative bias on the reported lactate result. the bias decreases over the in-use time, and depending on the amount of residue it may take anything between hours and days for the bias to disappear. worst case the bias upon membrane replacement is -1.5 mmol/l at lactate levels over 7.0 mmol/l. this is most apparent when comparing results measured before and immediately after membrane replacement.

Device

Lactate membrane units
  • Modèle / numéro de série
    The membrane units affected are: All lots of 942-066 When used on:ABL700 Series, and ABL800 Analyzers.
  • Description du dispositif
    measuring, Lactate, membrane, Analyzers
  • Manufacturer
    Radiometer Medical

Manufacturer

Radiometer Medical
  • Société-mère du fabricant (2017)
    Danaher Corporation
  • Représentant du fabricant
    Salehiya Trading Est., Riyadh, (01) 2628939
  • Source
    SFDA