Events

Retiro De Equipo (Recall) de SmartPump Tourniquet Pump

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Stryker Instruments Div. of Stryker Corporation.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    56624
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0913-2011
  • Fecha de inicio del evento
    2010-04-13
  • Fecha de publicación del evento
    2011-01-18
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2011-05-16
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=94405
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    Tourniquet, pneumatic - Product Code KCY
  • Causa
    This recall is related to the electri-cord recall. there is a risk when excessive force is applied to the plugs, a fracture can develop on the prongs inside the molded section of the plug. over time the fracture may lead to arcing inside of the molded section of the plug and a build up of heat which can cause charring, electric shock or fire. to this date there have been zero complaint for this.
  • Acción
    Stryker Instruments sent an Urgent - Medical Device Recall Notification letter dated April 13, 2010, to all affected customers. The letter identified the product, the problem,and the action to be taken by the customer. Stryker notified customers again on May 24, 2010, and again on September 14, 2010, via email, fax, or telephone. Customers were instructed to locate the units and visually inspect each affected cord. Remove the affected cord and dispose of it using their healthcare facilities disposal procedure. If the cord did not show signs of damage, the unit could remain in service until a replacement cord was available. Customers were to return the enclosed business reply form to confirm receipt of the notification letter and identify how many affected units were currently in their inventory. Stryker instruments would send out replacement cords. If the customer loaned or sold any of the units listed in the notification, the customer was to forward a copy of the notice to the new users and advise Stryker of the new user's name and their new location. If products were disposed of and were no longer in use, the customer was to advise Stryker of their obsolescence by providing them with their serial numbers. For questions regarding this recall call 800-800-4236, ext 3808 or ext 3584 Monday -Friday 8am-5pm (EST).

Device

SmartPump Tourniquet Pump
  • Modelo / Serial
    0732302333, 0732302343, 0732302353, 0732302363, 0733106963, 0735213703, 0735405473, 0735405474, 0735405483, 0800700973, 0800700983, 0800700993, 0800701003, 0800701013, 0801800723, 0801800733, 0801800743, 0803214363, 0803700403, 0803801283, 0803902253, 0804328223, 0804328233, 0804328243, 0804328253, 0804328263, 0811706053, 0811706063, 0812201033, 0814900313, 0814900323, 0815120633, 0815120643, 0819700663, 0819900233, 0819900243, 0819900253, 0821807013, 0822504833, 0822504843, 0822504853, 0824901913, 0824901923, 0826000313, 0826000323, 0826000333, 0826000343, 0827300013, 0827300023, 0827300033, 0829015213, 0829015223, 0829015243, 0829015253, 0835002033, 0835002043, 0835002053, 0835002063, 0901504783, 0901504793, 0901504803, 0902109543, 0906106523, 0907800563, 0907800573, 0907800583, 0907800593, 0908201653, 0908201663, 0908201673, 0908201683, 0910400813, 0911008053, 0911107753, 0911107763, 0911107773, 0911107783, 0911107793, 0911107803, 0911107813, 0911107823, 0911107833, 0911107843, 0914602763, 0914602773, 0914602783, 0914602793, 0914602803, 0916000173, 0916000183, 0916000193, 0916000203, 0916704763, 0916704773, 0916704783, 0916704793, 0918102513, 0918102523, 0918102533, 0918102543, 0918102553, 0918703413, 0918703423, 0918703433, 0918703443, 0920101133, 0920101143, 0920101153, 0920101163, 0920101173, 0920101183, 0921101213, 0921101223, 0921101233, 0921101243, 0922500993, 0922901853, 0922901863, 0922901873, 0922901883, 0922901893, 0922901903, 0922901913, 0922901923, 0924300113, 0924300123, 0924300133, 0924300143, 0924500963, 0924500973, 0924500983, 0924500993, 0924501003, 0924501013, 0925106953, 0925106963, 0929400403, 0929400413, 0930600863, 0930600873, 0930600883, 0930600893, 0930600903, 0930600913, 0930600923, 0930600933, 0930600943, 0930600953, 0934200463, 0934200473, 0934200483, 0934200493, 0935200423, 0935200433, 0935200443, 0935200453, 1001801033, 1001801043, 1001801053, 1001801063, 1001801073, 1005301213, 1005301223, 1005301233, 1005301243, 1005302123, 1005302133, 1005302143, 1006700063, 1006700073, 1006700083, 1006700093, 215753, 251753, 340503, 340504, 340512, 340514, 340515, 340518, 340520, 340522, 340524, 340528, 340533, 340534, 340536, 340537, 340538, 340544, 340546, 340549, 340550, 340551, 340553, 340554, 340556, 340557, 340558, 340559, 340561, 340562, 340563, 340564, 340566, 340570, 340572, 340573, 340574, 340575, 340576, 340583, 340585, 340598, 34060, 340600, 340602, 340603, 340604, 340605, 340606, 340607, 340611, 340614, 341000, 341001, 341002, 341003, 341004, 341009, 341011, 341012, 341013, 341014, 341015, 341016, 341017, 341018, 341019, 341020, 341021, 341023, 341024, 341025, 341026, 341027, 341028, 341029, 341030, 341031, 341032, 341033, 341034, 341036, 341039, 341040, 341042, 341044, 341048, 341053 and 341055.
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA (nationwide) and the countries of Portugal, Canada, China, Taiwan, France, Germany, Greece, Spain, India, Italy, Korea, Switzerland, Singapore, and England.
  • Descripción del producto
    Stryker Instruments, SmartPump Tourniquet System, Single Channel Tourniquet Pump, REF 5920-010-000, Rx only, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210. || Intended to be used to temporarily occlude or decrease blood flow in a patient extremity during a surgical procedure of that extremity.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation

Manufacturer

Stryker Instruments Div. of Stryker Corporation
  • Dirección del fabricante
    Stryker Instruments Div. of Stryker Corporation, 4100 East Milham Ave., Kalamazoo MI 49001
  • Empresa matriz del fabricante (2017)
    Stryker
  • Source
    USFDA