Events

Rappel de Device Recall MicroScan LabPro Information Manager System

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
    73417
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1269-2016
  • Date de mise en oeuvre de l'événement
    2016-02-11
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2018-01-04
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=144164
  • 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
    Medical device data system - Product Code OUG
  • Cause
    Beckman coulter is recalling the microscan labpro information manager system because the software incorrectly allows the operator to manually edit the carbohydrate substrates when manually reading dried overnight gram negative panels with an id hold status.
  • Action
    An Urgent Medical Device Recall Letter dated 2/11/2016 was sent to all customers who purchased the MicroScan LabPro Information Manager System, Version 1.0 to Version 4.41. Beckman Coulter is expanding the recall that was initiated in July 2015 regarding FA-25776 for the MicroScan LabPro Information Manager System. The letter informs the customers of the problems identified and the actions to be taken. Customers are instructed to complete and return the enclosed Response Form within 10 days. Customers with questions are instructed to contact Customer Support Representative: http:www.beckmancoulter.com, (800) 677-7226 in US and Canada. Customers outside of US and Canada, are instructed to contact their local Beckman Coulter representative.

Device

Device Recall MicroScan LabPro Information Manager System
  • Modèle / numéro de série
    not applicable
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Affected geographies: Bahamas, Belgium, Brazil, Canada, Chile, China, Colombia, Czech Republic, France, French Guiana, Germany, Ghana, Greece, Guadeloupe, Guatemala, India, Israel, Italy, Japan, Kazakhstan, Lithuania, Mexico, Morocco, Netherlands, Northern Mariana Islands, Panama, Paraguay, Peru, Poland, Portugal, Puerto Rico, Romania, Russia, Singapore, South Africa, Spain, Taiwan, Tunisia, Turkey, United States, Uruguay, Virgin Islands, Zimbabwe.
  • Description du dispositif
    MicroScan LabPro Information Manager System, Software Versions 1.0 to 4.41 || Catalog No. 10638819, 10638820, 10638823, 10638824, 10638825,10638826, 10714149,10714159, 10805072, 10805073, 10975000, 10975001, 6000-0008, 6000-0026. || Japan: || 10638819 LabPro v4.11 Software Update Kit || 10638820 LabPro v4.11 System Software || 10805072 LabPro MBT Non-Connect Systems v4.30 || 10805073 LabPro MBT Connect Systems v4.30 || Canada: || 6000-0008 LabPro v4.41 Panel Update-06 Kit || 6000-0026 LabPro Connect v4.41 Panel Update-06 Kit || 10638823 LabPro v4.11 Software Update Kit || 10638825 LabPro v4.11 System Software || 10638824 LabPro v4.11 Software Update Kit || Europe: || 10638824 LabPro v4.11 Software Update Kit || 10638826 LabPro v4.11 System Software || USA: || 10714149, LabPro v4.11 Software Update Kit || 10714150 LabPro v4.11 System Software || 10975000 ASM LabPro-MBT v4.40 || 10975001 ASM LabPro-MBT v4.40 for Connect || 6000-0008 LabPro v4.41 Panel Update-06 Kit || 6000-0026 LabPro Connect v4.41 Panel Update-06 Kit || ROW: || 6000-0008 LabPro v4.41 Panel Update-06 Kit || 10638823 LabPro v4.11 Software Update Kit || 10638825 LabPro v4.11 System Software || 10638824 LabPro v4.11 Software Update Kit || 10638826 LabPro v4.11 System Software || Product Usage: || LabPro Data Management System is a Microsoft Windows based software program and is intended to manage both microbial identification (ID) and antimicrobial agent susceptibility testing (AST) data generated from MicroScan instruments or manually entered microbiology test results, for use by trained laboratory personnel. LabPro AlertEx is a functional subset of the LabPro Data Management System that analyzes MicroScan ID and AST data, or other predefined parameters, against a series of established rules/alerts and notifies the user of unusual and/or critical conditions, which may warrant further analysis or actions.
  • 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