Rappel de Device Recall OPTIGEN Food 30

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Hitachi Chemical Diagnostics Inc.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    64132
  • Classe de risque de l'événement
    Class 3
  • Numéro de l'événement
    Z-0793-2013
  • Date de mise en oeuvre de l'événement
    2012-12-21
  • Date de publication de l'événement
    2013-02-07
  • Statut de l'événement
    Terminated
  • Pays de l'événement
  • Date de fin de l'événement
    2013-05-16
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    System, test, radioallergosorbent (rast) immunological - Product Code DHB
  • Cause
    There is no evidence that a visual inspection was performed on one tray of coverslips. possibility of a low fill volume which could lead to a false negative results.
  • Action
    Hitachi sent an Urgent Product Recall Notification letter dated December 21, 2012, to the affected customer. The letter identified the product, the problem, and the action to be taken by the customer. The customer was instructed to discontinue distribution and destroy any remaining inventory of the affected product at their location per their local waste ordinances, determine if any of their customers are using or have inventory of the affected product, rquest that their customers review all patient results reported with the use of the affectted product. The customer was instructed to tell their customers to discontinue use and destroy any remaining inventory per their local waste ordinances. The customer was instructed to retain a copy of the notification letter for their records. The customer was also instructed to send confirmation of the destruction within 5 days Customers were instructed to complete and return the attached Certificate of Destruction. For questions customers were instructed to contact their local area Customer Service. For questions regarding this recall 650-961-5501.

Device

  • Modèle / numéro de série
    Catalog number: 85035. Lot number 42K283626, expiration May 31, 2013.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - France only
  • Description du dispositif
    OPTIGEN Food 30; Catalog number: 85035. For allergen testing. || Manufactured by Hitachi Chemical Diagnostics, Mountain View, CA. || Distributed by Theridiag, Cedex, France
  • Manufacturer

Manufacturer

  • Adresse du fabricant
    Hitachi Chemical Diagnostics Inc, 630 Clyde Ct, Mountain View CA 94043-2239
  • Société-mère du fabricant (2017)
  • Source
    USFDA