Events

Rappel de Device Recall Terumo Pall AL6X Arterial Blood Line Filter

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 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
    65981
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2261-2013
  • Date de mise en oeuvre de l'événement
    2013-07-26
  • Date de publication de l'événement
    2013-09-20
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2015-07-28
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=121140
  • 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
    Filter, blood, cardiopulmonary bypass, arterial line - Product Code DTM
  • Cause
    Medical device used in cardiovascular procedures is defective.
  • Action
    Terumo Cardiovascuolar Services sent recall letters to Chief of Perfusion, Director of Operating Room Services, Director of Biomedical Services, and Risk Management departments on July 26, 2013. The notifications advised that filters are being recalled because some of the filters may exhibit a partial or full occlusion of an outlet or purge port. Terumo CVS advised users to stop using Terumo AL6X arterial filters from the affected lot numbers for replacement. A supply of replacement filters for customer's immediate use accompanied the notification. For users ordering the AL6X filters as part of a Cardiovascular Procedure Kit, Terumo CVS is providing a preliminary supply of replacement Terumo AL6X arterial filters in which users may follow the instructions to replace the filter or users may return the Cardiovascular Procedure Kit and Terumo CVS will replace the filter for them. Customers with questions were advised to contact Terumo CVS Customer Service at 800-521-2818. For questions regarding this recall call 800-521-2818.

Device

Device Recall Terumo Pall AL6X Arterial Blood Line Filter
  • Modèle / numéro de série
    Recalled filters sold singly are identified with Part Number AL6X with the following lot codes:  MM19,  MN23,  NC15,  ND01,  ND08,  ND29,  NE11,  NE18,  NE25,  NF09,  NF31,  PA23,  PD05,  PE02,  PF14,  PF21,  PG04,  PG11,  PG18,  PG25,  PH09,  PH16,  PH30,  PK06,  PK13,  PL24,  PM01,  PM08,  PM22,  PM29,  PN12,  PN26,  PP17,  PP31,  QA07,  QA14,  QA21,  QC04,  QC25,  QD11,  QD18,  QD25,  QE08,  QE15,  QE22,  QE29,  QF06,  QF28, MM26,  NL12,  NM24,  NP12, and PA30;    Affected filters, also Part # AL6X, packaged within Terumo Cardiovascular Convenience Kits are identified with the following lot codes:  PN19,  QA14,  QC11R,  QD04,  QE15,  QF06,  QF13,  NM31,  NP05,  PC20,  PD05,  QF28,  QC04,  PD26,  PG04,  PE23R,  PK13,  PK20,  QA21,  QC11,  QC11A,  QD11,  QE01,  PL17,  QE08,  NK08,  PG25,  PN26,  QC18,  NN07,  NN07R,  PA16,  PA16R,  PC27,  PC27R,  PF07,  PL24,  PD12,  PE09,  PE30,  PH09,  PL10,  PE23,  PF14,  PG18,  PK06,  PM01,  PM22,  PN12,  QA02,  QA28,  QC25,  QD25,  NK01,  NK08R,  PH23,  PH16,  PL10A,  PM15,  PP10,  PP17,  QD18,  QE22,  NM17,  NM17A,  PC06,  PC06R,  PE09R,  QE01A,  QE15A,  QE15T,  QE15TA,  QE15TC,  QF13T,  QF20,  QF20T,  NA10R,  NA17R,  ND14,  ND28,  ND28T,  NE11T,  NE18,  NF23,  NG06,  NG20,  NH11,  NH18,  NK15,  NL12,  NL26,  NM03,  NM10,  NM24,  NN14,  NN28,  NP12,  PA30,  PC13,  PD19,  PE16,  PF07A,  PF21,  PK27,  PK27A,  PL04,  PM08,  PP03,  QA14T,  QE29,  QF28T,  QF28TA,  PG11,  PH30,  PH30A,  PN26A,  QA07,  NH25,  NK29,  PE02,  PF29,  PN19,  QG17,  PK13A,  QD11A,  MN22,  NE25,  NF31,  PM29,  PA09,  QG03,  PA02,  PH23T,  PG11T,  QC18R,  QF06A,  PH09T,  PH09TA,  QF13TA,  QF20TA, and QF20TC
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including WA, IN, OK, TX, MI, CA, NY, CT, AZ, FL, WV, NC, VA, PA, TN, GA, AL, MA, SC, OH, MS, MO, SD, WI, AR, AND NV.
  • Description du dispositif
    Terumo Pall AL6X Arterial Blood Line Filter, labeled in part Terumo Cardiovascular Systems Corporation, packaged as part of a Terumo Cardiovascular Procedure Kit or as a single, sterile filter unit || Single/Sterile Terumo Pall AL6X Arterial Filter: The Terumo Pall AL6X Arterial Filter is indicated for use in cardiopulmonary bypass procedures for the removal of micro-emboli greater than 40 microns in size, including gas emboli, fat emboli and aggregates composed of platelets, red blood cells and other debris from the arterial line and where the flow rate will not exceed 8 liters per minute. Cardiovascular Procedure (Convenience) Kit that includes the Terumo Pall AL6X Arterial Filter: The Cardiovascular Procedure Kits are indicated for use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed. The sterile cardiovascular procedure kit is intended to be used one time for periods up to 6 hours.
  • Manufacturer
    Terumo Cardiovascular Systems Corporation

Manufacturer

Terumo Cardiovascular Systems Corporation
  • Adresse du fabricant
    Terumo Cardiovascular Systems Corporation, 125 Blue Ball Rd, Elkton MD 21921-5315
  • Société-mère du fabricant (2017)
    Terumo Corp.
  • Source
    USFDA