Events

Rappel de Device Recall Terumo Custom Cardiovascular Kits

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 Terumo Cardiovascular Systems Corp.

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
    74856
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2706-2016
  • Date de mise en oeuvre de l'événement
    2016-07-25
  • Statut de l'événement
    Open, Classified
  • Pays de l'événement
    United States
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=148609
  • 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
    Cardiovascular procedure kit - Product Code OEZ
  • Cause
    Terumo custom cardiovascular procedure kits are labeled as xcoating surface coated tubing, but tubing is non-coated.
  • Action
    Terumo Cardiovascular Systems issued the Safety Alert dated July 25, 2016 and advises the user that their kit may include uncoated tubing, and further advises the consignee to continue using their kits with consideration of anticoagulation protocols during a procedure. Each consignee is asked to complete a Customer Response Form, and to return the Customer Response Form to Terumo acknowledging their receipt of the form. Consignees can return their affected product for credit/replacement; however, return of the product from the field is a customer option and is not under recommendation from Terumo Cardiovascular Systems. For further questions, please call (800) 262-3304.

Device

Device Recall Terumo Custom Cardiovascular Kits
  • Modèle / numéro de série
    US Lot Codes: UG06  UE18R  UF31  UF31A  UF31T    UG13  UG13A  UG20  UG20T  UG27  UG27T   OUS Lot Codes:  UG13  UG13T  UG20  UG20T
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Foreign: Canada, Latin America
  • Description du dispositif
    Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled containing Coated Tubing as follows: || This product is intended for use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it. This product is a sterile, disposable kit, intended for one-time use for periods up to 6 hours, after which it must be discarded in a manner which is within applicable laws and practices. Terumo Cardiovascular System Cardiovascular Procedure Kits. Each kit is assigned a unique product code/catalog number that is specific to the consignee who has established specifications for the kit. || US Product Codes: || 72021 || 72358 || 71180-01 || 76021 || 76022 || 76023 || 76024 || 76025 || 71801-01 || 71801-01 || 71801-01 || 71801-01 || 71801-01 || 74163-03 || 71296-01 || 74460-01 || 74460-01 || 74460-01 || 73208-03 || 74382-01 || 74382-01 || 74382-01 || 74916 || 74916 || 74916 || 70089-07 || 74063-01 || 74063-01 || 74460-01 || 74460-01 || 74460-01 || 74460-01 || 75252-01 || 74951 || 75881 || 74271-01 || 71085-02 || 72742 || 75314 || 75368 || 75368 || 76095 || 76095 || 73339-01 || 73789 || 74417 || 72204 || 72965-03 || 73644 || 73645-01 || 73700 || 73861 || 73871 || 73901-03 || 75612 || 75617 || 75986 || 76095 || 73645-01 || 73645-01 || 70099-04 || 75544 || 75272 || 75674 || 75674 || 73180 || 73180 || 73180 || 75437 || 75674 || 75274 || 73811 || 73811 || 74915 || 71175-03 || 73738 || 76117 || 75129 || 75642 || 75642 || 72596 || 72596 || 72596 || 75179 || 74980-01 || 8340TXC-07 || 8340TXC-07 || 8340TXC-07 || 71875-01 || 74235-01 || 74476 || 75059 || 75547 || 75547 || 74235-01 || 8351TXC-01 || 73124 || 73281-01 || 73282-01 || 73874 || 74477 || 8340TXC-07 || 76069 || 76070 || 76071 || 76072 || 74737 || 73933 || 73933 || 73933 || 73933 || 73933 || 73933 || 71608-04 || 75413 || 74959 || 75472 || 75472 || 75449 || 75923 || 75923 || 73729-01 || 73730-01 || 74046-
  • Manufacturer
    Terumo Cardiovascular Systems Corp

Manufacturer

Terumo Cardiovascular Systems Corp
  • Adresse du fabricant
    Terumo Cardiovascular Systems Corp, 28 Howe St, Ashland MA 01721-1305
  • Société-mère du fabricant (2017)
    Terumo Corp.
  • Source
    USFDA