Events

Rappel de Device Recall Sarns Modular Perfusion System 8000

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
    60774
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1453-2012
  • Date de mise en oeuvre de l'événement
    2012-03-21
  • Date de publication de l'événement
    2012-04-23
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2013-07-11
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=108162
  • 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
    Console, heart-lung machine, cardiopulmonary bypass - Product Code DTQ
  • Cause
    Terumo received multiple reports of malfunctions of the cardioplegia and arterial monitors for the sarns modular perfusion system 8000. upon review of complaint investigation, the malfunctions are caused by or could have been caused by soldering anomalies on the circuit board of the monitor. the compromised solder joints could cause intermittent or loss of display, or could cause monitor reset, po.
  • Action
    TERUMO sent an URGENT MEDICAL DEVICE RECALL- SAFETY ADVISORY to all consignees on March 21, 2012 via Federal Express. Terumo issued the safety advisory to remind users how to intervene if they experienced intermittent or complete loss of pressure display on the arterial monitor or cartiplegia monitor, or a related pump stop. Customers were asked to review the Medical Device Correction notice, assure that all users are aware of the notice, confirm receipt of the communication by faxing the attached Customer Response Form to 1-800-292-6551. For questions regarding this recall call 1-800-521-2818.

Device

Device Recall Sarns Modular Perfusion System 8000
  • Modèle / numéro de série
    Catalog Number 16413; Lot numbers/serial numbers: 1, 2, 3, 246553, 249652, 253943, 256867, 258565, 263614, 269567, 276866, 279012, 281191, 288150, 290070, 296227, 298374, 303142, 308343, 309896, 320618, 323004, 325187, 327295, 329342, 330149, 331788, 333055, 335139, 337482, 341259, 343978, 349845, 352311, 355122, 358382, 358383, 360213, 367161, 370516, 376523, 378092, 381115, 383781, 389150, 392116, 395215, 400085, 400086, 400833, 401042, 401570, 401675, 402124, 402264, 403141, 403142, 403545, 403712, 403719, 404180, 404359, 405057, 405333, 405712, 405859, 406219, 406366, 406512, 406717, 407049, 407241, 407338, 407620, 407637, 407813, 407902, 408362, 408526, 408666, 409214, 409283, 409297, 409422, 409571, 410057, 410250, 410397, 411130, 411208, 411295, 411563, 412058, 412213, 412890, 413161, 413182, 414317, 414363, 414815, 415034, 415250, 415670, 416854, 417128, 417433, 417435, 417561, 418217, 418779, 418911, 419146, 419556, 420313, 420687, 421632, 421834, 422083, 422739, 423663, 424267, 426877, 429622, 430398, 438156, 439123, 444234, 445779, 448180, 452751, 455760, 458517, 461157, 463964, 467455, 468739, 479124, 483205, 483635, 487380, 9434006, 93326004, 94059004, 94115004, 94123004, 94123005, 94130005, 94143005, 94143006, 4158005, 94175005, 94179005, 94179006, 94186005, 94186006, 94200005, 4200006, 94206005, 94206006, 94234006, 94249006, 94284006, 94297006, 94304006, 94311006, 94318006, 95006005, 95048006, 95059006, 95067006, 95086006, 95094006, 95108006, 95114006, 95122006, 95171006, 95174006, 95215006, 95223006, 95234006, 95244006, 95265006, 95282006, 95305006, 95312006, 95345006, 95356006, 96043006, 96091 006, 961 03006, 961 08006, 96143008, 96158008, 96162008, 96200008, 96228008, 96236008, 96241008, 96253008, 96277008, 96295008, 96313008, 96344008, 96348008, 96353008, 97004008, 97006008, 97007008, 97052008, 97066008, 97087008, 97113008, 97120008, 97132008, 97141008, 97156008, 97157008, 97161008, 97199008, 97223008, 97230008, 97238008, 97261008, 97279008, 97302008, and 97308008.
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - USA including AK, AL , AR, AZ , CA, CO , CT, DC, DE , FL, GA, HI, IA , ID , IL, IN , KS, KY , LA, MA , MD, MI, MN , MO, MS , MT, NC , ND, NE, NH, NJ, NM , NY, OH , OR, PA , RI, SC , TN, TX , VA, WA , WI, WV, WY, and Puerto Rico and the countries of PERU, Philippines, REPUBLICA, SANTIAGO, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sri Lanka, Switzerland, Taiwan, Thailand, Tujunga, United Arab Emirates, Uruguay, Venezuela, Vietnam, Wooddale, and Yemen.
  • Description du dispositif
    Sarns Modular Perfusion System 8000 Catalog number 149112 or 78-8067-4840-2 Temperature-Pressure Board, Arterial Monitor (service part only) || The 8K Arterial Monitor is intended for use with the 8000 Modular Perfusion System to display one average pressure and three average temperatures and also provide two digital timers. The pressure channel can have alert and alarm levels set by the user to indicate overpressure conditions. The alert and alarm level settings are retained by the system and can be recalled after the next power up. Alert and alarm conditions are indicated by flashing LED bar with single or dual audio tones; an alarm will also stop the arterial and cardioplegia pumps.
  • Manufacturer
    Terumo Cardiovascular Systems Corporation

Manufacturer

Terumo Cardiovascular Systems Corporation
  • Adresse du fabricant
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Road, Ann Arbor MI 48103-9586
  • Société-mère du fabricant (2017)
    Terumo Corp.
  • Source
    USFDA