Rappel de Xpert BCR-ABL Monitor assay (used for monitoring patients being treated for chronic myelogenous leukaemia). An in vitro diagnostic medical device (IVD).

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Cepheid Holdings Pty Ltd.

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
    RC-2017-RN-00083-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2017-01-20
  • Pays de l'événement
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
  • Notes / Alertes
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Notes supplémentaires dans les données
  • Cause
    Internal tests conducted by cepheid show that certain lots of xpert bcr-abl monitor (bcr-100n-10) meet performance claims up to 12 months after the date of manufacture instead of the current expiration dating (up to 24 months). assay stability data beyond 13 months under reported the amount of bcr-abl mrna transcript at the lowest level. the claimed performance for the assay allows for a 2-fold variance in the ratio of bcr-abl to abl mrna transcripts whereas at 25 months a 3-fold difference was observed. at 13 months a 1.8-fold variance was observed, which is within the claimed product performance variability. although outside of the stability limits, the detected level of bcr-abl mrna transcript is correctly called as bcr-abl detected.The expiry dates of affected lots have changed to reflect the new 12 month timeframe. as a result, lot 1000026629 expired as of 4 jan 2017, and lot 1000027258 and 1000040993 will expire in march 2017 and august 2017, respectively.
  • Action
    Cepheid is advising, based on the assignment of the new expiry date, that Xpert BCR-ABL Lot 1000026629 (Cartridge Lot 21503) expired on 4 Jan 2017. Customers are to stop using and dispose of product from this lot. Cepheid will provide replacement product. Results obtained using this lot from tests run after 4 Jan 2017 should be reviewed for outliers not associated with known clinical factors (eg. therapy compliance). For Lot 1000027258 (Cartridge Lot: 21703) and Lot 1000040993 (Cartridge Lot: 22402), the new expiry dates are 1 Mar 2017 and 15 Aug 2017, respectively. Customers are to stop using and dispose of remaining product from these lots after the newly assigned expiry dates. Cepheid will provide replacements for product remaining after the new expiry dates. This action has been closed-out on 28/02/2018.

Device

  • Modèle / numéro de série
    Xpert BCR-ABL Monitor assay (used for monitoring patients being treated for chronic myelogenous leukaemia). An in vitro diagnostic medical device (IVD).Catalogue Number: BCR-100N-10Lot Number: 1000026629 (Cartridge Lot: 21503)Expiry on label: 9 Apr 2017Lot Number: 1000027258 (Cartridge Lot: 21703)Expiry on label: 9 Apr 2017Lot Number: 1000040993 (Cartridge Lot: 22402)Expiry on label: 25 Feb 2017ARTG Number: 226631
  • Manufacturer

Manufacturer