Events

Rappel de Device Recall IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent

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 Beckman Coulter 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
    63152
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0003-2013
  • Date de mise en oeuvre de l'événement
    2012-01-27
  • Date de publication de l'événement
    2012-10-01
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2013-05-30
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=112693
  • 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, rheumatoid factor - Product Code DHR
  • Cause
    The recall was initiated because beckman coulter has confirmed customer reports of qc shifts, lot-to-lot variation, and an increase in the percent of patient samples recovering >20 iu/ml using the lots# m012376 and m101865 of immage rf reagent. the lots identified for the rf reagent might produce false abnormal results.
  • Action
    The firm, Beckman Coulter, sent an "URGENT PRODUCT CORRECTION" letter dated January 27, 2012 with an attached PCA Response Form to all customers who purchased the IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent. The letter describes the product, problem and actions to be taken. The customers were instructed to discontinue use of IMMAGE RF reagent lots M012376 and M101865; call Order Assistance at (800) 526-3821 in the United States, (800) 463-7828 in Canada or contact your local Beckman Coulter representative for replacements; and complete and return the enclosed FAX BACK RESPONSE FORM within 10 days via mail at: Beckman Coulter, Inc., 250 S. Kraemer Blvd, Mail Stop A2.0246, Brea, CA 92822-8000; Attn: Regulatory Affairs or fax to: (714) 961-4234. Note: Beckman Coulter has added additional release testing that will assure future lots RF will meet the reference interval claim of the IMMAGE RF Instructions for Use (IFU). If you have any questions concerning this letter, contact Beckman Coulter Support Center (call Center) on the Beckman Coulter Website at: http://www.beckmancoulter.com/customersupport/support/ or call (800) 854-3633 in the US and Canada. Outside of the US and Canada, customers were instructed to contact their local Beckman Coulter Representative.

Device

Device Recall IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent
  • Modèle / numéro de série
    Lot# M012376 and M101865
  • Classification du dispositif
    Immunology and Microbiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution: USA (nationwide) and country of: Canada.
  • Description du dispositif
    IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent, PN 447070 || The IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) reagent, in conjunction with Beckman Cal 5 Plus, is intended for use in the quantitative determination of human rheumatoid factor concentrations in human serum and plasma samples by rate nephelometry. This assay is designed for use with the IMMAGE Immunochemistry System.
  • Manufacturer
    Beckman Coulter Inc.

Manufacturer

Beckman Coulter Inc.
  • Adresse du fabricant
    Beckman Coulter Inc., 250 S Kraemer Blvd, Brea CA 92821-6232
  • Société-mère du fabricant (2017)
    Danaher Corporation
  • Source
    USFDA