Retiro De Equipo (Recall) de Device Recall SOL SYS 8IN CALCAR SZ12

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 DePuy Orthopaedics, Inc..

¿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
  • ID del evento
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
  • Fecha de inicio del evento
  • Fecha de publicación del evento
  • Estado del evento
  • País del evento
  • Fecha de finalización del evento
  • Fuente del evento
  • URL de la fuente del evento
  • 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
    Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented - Product Code LPH
  • Causa
    An engineering analysis has determined the solution calcar stem has the potential to result in impingement with a variety of heads. this impingement may not allow the stem and head to lock as intended. the amount of possible impingement varies depending on the femoral head. worst case condition: calcar stem with -2mm offset articuleze maximum of 0.937mm radial impingement. it is evident that a.
  • Acción
    Deputh Orthopaedics sent an Urgent Information - Medical Device Recall Notice dated December , 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. The notification letter instructed consignees to please cease further distribution or use of products immediately. The purpose of the communication was to inform them of this recall and request acknowledgement of receipt of this letter by their facility. Reconciliation forms should be returned to your DePuy Sales Representative or faxed to the following Fax Number: 574-371-4939. For questions regarding this recall call 574-267-8143.


  • Modelo / Serial
    Product Code: 157215121 and Lot codes: 105800, 132795, 134667, AB8D51000, AB8D5A, AB8HE1000, AB8HE1A, AE3L11000, AF1EP1000, AF1EP1A, AF7KK1000, AV7JW1000, AW8F21000, AW8F2A000, BR4J81000, C15AN1000, C34B61000, C61CA1000, C77A81000, CE6FF1000, CE6FK1000, CG5B41000, CG5B41A, CK6BN1000, CK6BP1000, CK6BPA000, D32J41000, D46LD1000, D58EW1000, D74FB1000, DD3BP1000, DG1N71000, DH9JV1000, DH9JVA000, DW2A11000, E1RHD1000, E3SDC1000, E45LR1, E51E11, EB4MY1000, ED1DF1000, EH6B31000, ET4FG1000, EW7CD1000, FD4SW1, FJ9L71, and FK9D11.
  • Clasificación del producto
  • Clase de dispositivo
  • ¿Implante?
  • Distribución
    Nationwide Distribution including AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WY and GUAYNABO, PR
  • Descripción del producto
    SOL SYS 8IN CALCAR SZ12 || Packaging: Product is packed within a poly protector, with protection added as needed for fragile points. The entire stem is then placed within a foam sleeve for added protection. The assembly is then placed and sealed in an inner and outer tray for aseptic transfer. The sealed package is placed into a folding carton, labeled, and shrink wrapped. || Intended Use: SOLUTION System Calcar Stems are used in total hip arthroplasty (THA) to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components.
  • Manufacturer


  • Dirección del fabricante
    DePuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
  • Empresa matriz del fabricante (2017)
  • Source