Events

Rappel de Device Recall DPM Central Monitoring 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 Mindray DS USA, Inc. d.b.a. Mindray North America.

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
    64114
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0798-2013
  • Date de mise en oeuvre de l'événement
    2012-11-28
  • Date de publication de l'événement
    2013-02-11
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2013-08-15
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=115379
  • 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,network and communication,physiological monitors - Product Code MSX
  • Cause
    Mindray has identified a software anomaly that may where, in the presence of an asystole, the telepack ecg waveform may produce a unique step pattern (instead of a flat line) if lead 1 or v is being utilized for detecting cardiac arrhythmia.
  • Action
    Mindray North America/ Mindray DS USA Inc. sent an "URGENT PRODUCT CORRECTION ACTION" letter dated November 28, 2012 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. Contact your Mindray Service Representative at 1-800-288-2121 for questions relating to this issue.

Device

Device Recall DPM Central Monitoring System
  • Modèle / numéro de série
    Part No Serial No 300BF-PA00002 EH-17000037 300BF-PA00002 EH-17000032 300BF-PA00002 EH-17000033 300BF-PA00002 EH-25000099 300BF-PA00002 EH-18000043 300BF-PA00003 EH-1A000072 300BF-PA00002 EH-22000088 300BF-PA00003 EH-1A000073 300BF-PA00002 EH-12000060 300BF-PA00002 EH-17000038 300BF-PA00003 EH-21000077 300BF-PA00002 EH-18000058 300BF-PA00002 EH-23000096 300BF-PA00003 EH-19000059 300BF-PA00003 EH-19000060 300BF-PA00002 EH-18000051 300BF-PA00002 EH-12000054 300BF-PA00002 EH-16000029 300BF-PA00002 EH-11000052 300BF-PA00002 EH-17000039 300BF-PA00003 EH-1A000064 300BF-PA00002 EH-18000050 300BF-PA00003 EH-13000078 300BF-PA00003 EH-13000085 300BF-PA00002 EH-18000053 300BF-PA00002 EH-17000036 300BF-PA00002 EH-17000031 300BF-PA00003 EH-17000040 300BF-PA00002 EH-18000054 300BF-PA00002 EH-1A000069 300BF-PA00002 EH-12000062 300BF-PA00002 EH-21000076 115-006908-04 Software Kit 300BF-PA00003 EH-13000083 300BF-PA00003 EH-13000084 300BF-PA00003 EH-22000087 300BF-PA00002 EH-18000056 300BF-PA00002 EH-17000035 300BF-PA00002 EH-18000048 300BF-PA00002 EH-18000052 300BF-PA00003 EH-21000081 300BF-PA00002 EH-17000030 115-006908-03 Software Kit 115-006908-03 Software Kit 115-006908-03 Software Kit 300BF-PA00003 EH-19000062 300BF-PA00002 EH-18000057 300BF-PA00003 EH-22000083 300BF-PA00002 EH-11000051 300BF-PA00002 EH-18000041 300BF-PA00002 EH-21000082.
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Mindray DS USA, Inc., DPM Central Monitoring System with ambulatory Telepack. Part numbers: 300BF-PA00002, and 300BF-PA00003 (DPM Central Monitoring System) 115-006908-01, -03, -04 (DPM software upgrade kit). The DPM Central Monitoring System transfers information between DPM Central station and other networked devices.
  • Manufacturer
    Mindray DS USA, Inc. d.b.a. Mindray North America

Manufacturer

Mindray DS USA, Inc. d.b.a. Mindray North America