Events

Rappel de Device Recall Cable Assembly for the RIO STANDARD 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 Mako Surgical Corporation.

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
    53033
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0064-2010
  • Date de mise en oeuvre de l'événement
    2009-07-17
  • Date de publication de l'événement
    2009-10-19
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2010-05-12
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=84483
  • 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
    Neurological Stereotaxic Instrument - Product Code HAW
  • Cause
    Cables fail to provide adequate transmission. mako surgical corporation is recalling 200996 cable assembly, hybrid extended length; 200997 cable assembly, hybrid, guidance module; and 200998 cable assembly, hybrid, ui panel. these parts are sub components of the 20300 rio standard system.
  • Action
    A Recall Notice, dated July 15, 2009, was sent to owners of the RIO system (hospital OR staff) with a signed acknowledgement returned to MAKO. Surgeons using the RIO system during the recall time period, regardless of whether their system has already been upgraded, are given the notification letter and asked to sign and return the acknowledgement memo. The letter stated that customers' RIO will be upgraded to replace the potentially faulty cable with a new cable. Their MAKOplasty Specialist (MPS) will notify them when their system was scheduled to have their fiber optic cable upgrade. The upgrade will be installed by a Field Service Engineer (FSE) free of charge and the RIO will be completely tested prior to being returned to service. Customers should direct questions or concerns to their MPS, FSE, or Jim Pomeroy, who can be reached at 954-927-2044.

Device

Device Recall Cable Assembly for the RIO STANDARD SYSTEM
  • Modèle / numéro de série
    Serial Numbers: ROB031 through ROB068.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    200996-Cable Assembly, Hybrid Extended Length, || 200997 Cable Assembly, Hybrid, Guidance Module, || 200998 Cable Assembly, Hybrid, UI Panel || Subcomponents for the 203000 RIO STANDARD SYSTEM || Manufactured by: MAKO Surgical, Corp. Fort Lauderdale, FL. || All three cables are integral components and are not purchased separately. || However, 200996-Cable Assembly is the only cable visible. This cable is labeled: 200996-REV-1, KSM 390634-1, SN 000001. 200997 and 200998 Cable Assembly are not visible . || The Tactile Guidance System v2.0 is intended to assist the surgeon in providing software defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.
  • Manufacturer
    Mako Surgical Corporation

Manufacturer

Mako Surgical Corporation
  • Adresse du fabricant
    Mako Surgical Corporation, 2555 Davie Rd Ste 110, Davie FL 33317-7424
  • Source
    USFDA