Events

Avis De Sécurité sur LIFECODES Quik-ID Class II (CZID)

Selon Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), ce/cet/cette avis de sécurité concerne un dispositif en/au/aux/à Slovenia qui a été fabriqué par Immucor GTI Diagnostics, Inc..

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
    Field Safety Notice
  • Date
    2016-01-08
  • Pays de l'événement
    Slovenia
  • Source de l'événement
    AMPMDRS
  • Notes / Alertes
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Notes supplémentaires dans les données
  • Cause
    We have determined that the lifecodes quik-ld class ii lot indicated above may generate invalid assays due to high negative serum control (nc) values. per the lifecodes quik-id class ii instructions for use (ifu), the average negative control value must be <_0.225 od. an increase of the nc average od above this limit would result in a failed assay. where the nc is increased without achieving values above this limit, samples may demonstrate false negative results (borderline reactivity) at or near the cutoff for the assay.

Device

LIFECODES Quik-ID Class II (CZID)

Manufacturer

Immucor GTI Diagnostics, Inc.