Alerte De Sécurité sur 100 ml Test Kit - Pearls 100u./Reagent 1x7,5mL / Adjusters mL (lyophilized) 2x4mL (commercially available) Product Name: IGF-I - IMMULITE (Anvisa Record No. 10345161109) /// Affected Model (s) / Solution 1x30mL /// Affected lot: 411 /// Product risk class: II.

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par Siemens Healthcare Diagnósticos S.A.; Siemens Healthcare Diagnostics Products Ltd...

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Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

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  • Type d'événement
    Safety alert
  • ID de l'événement
    1896
  • Date
    2016-05-11
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 data from the U.S. and Brazil.
  • Notes supplémentaires dans les données
    AT.
  • Cause
    Siemens healthcare diagnostics has identified that incubation prior to the processing of patient samples takes 24 minutes in the immulite / immulite 1000 system so that the pretreatment solution reaches full equilibrium when using the pre-treatment solution (lgfa) lot 055 , contained in the immulite 2000 igf-i kit, batch 411. if patient samples are processed before full equilibrium is reached, an underestimate recovery of -36% may occur. however, if the sample is incubated for more than 24 minutes before the test, an underestimate will not be observed. there is a potential for a falsely suppressed igf-i value that may delay the diagnosis for acromegaly and / or potential pharmacological treatment to normalize serum igf-i. the impact of clinical potential is mitigated by serum igf-i monitoring as well as by correlation of serum growth hormone dosages and clinical presentation. quality controls will not detect this problem.
  • Action
    Field classification: letter to the client /// Field action code: IMC 16-05 /// Recommendations to users and patients: ensure that the pre-treatment solution is incubated with the patient sample for at least 24 minutes prior to processing in the IMMULITE / IMMULITE 1000 systems.

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