Retiro De Equipo (Recall) de Device Recall Extreme Custom

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 Ossur H / F.

¿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
    73380
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1297-2016
  • Fecha de inicio del evento
    2016-02-24
  • Estado del evento
    Terminated
  • País del evento
  • Fecha de finalización del evento
    2016-08-15
  • Fuente del evento
    USFDA
  • 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
    Orthosis, limb brace - Product Code IQI
  • Causa
    Ossur americas is recalling , knee shield / patella cup, knee undersleeve gray, necloc extrication collar, rebound cartilage, rebound cartilage custom, rebound air walker, rebound diabetic walker, back support suspenders clip on black, back support suspenders sew on black, extreme custom, unloader custom xt, unloader custom lite, unloader custom, and papoose infant spine immobilizers because the p.
  • Acción
    The firm sent out customer notification letters on 02/26/16. The notification letter instructed customers to include the latex caution notice in any existing inventory of affected products. The latex caution notice can be retrieved at the conclusion of the response survey or by going directly to safetyalerts.ossur.com. Should customers require ¿ssur to provide pre-printed notices for existing inventory, contact ¿ssur customer service. For the ¿ssur Miami J¿ Cervical Collars with lot numbers before MX150727 customers are instructed to remove and discard the assist strap, which contains natural rubber latex, located in the patient pack. Recipients of the notice with should take the following actions: 1. Pass the notice to those who need to be aware within the organization or to any organization where the affected devices have been transferred. 2. Maintain awareness on this notification for an appropriate period. 3. If have further distributed the products, identify customers and notify them at once of the product alert. It is recommended to include a copy of the alert notification letter. 4. If any of your customers are currently wearing a product, check for any skin irritations or other reactions consistent with natural rubber latex allergies. 5. To verify have received the notification, visit safetyalerts.ossur.com to complete the Response Survey. If any questions, contact ¿ssur Customer Service at (800) 233-6263. The notification letter for the Papoose Infant Spine Immobilizer contained the following additional actions/instructions: Examine inventory, quarantine products subject to the recall and contact customer service for a return authorization to return the product to ¿ssur. If any of customers are currently wearing a product, it is recommended replacing the unit with one shipped after the transition lot number MX150727. Check for any skin irritations or other reactions consistent with natural rubber latex allergies.

Device

  • Modelo / Serial
    Item No: B-108500010 B-108500020 B-108600010 B-108600020 B-123500020 B-123600020
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    U.S. distribution to the following; 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, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Descripción del producto
    Extreme Custom || Product Usage: || Extreme Custom is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
  • Manufacturer

Manufacturer

  • Dirección del fabricante
    Ossur H / F, Grjothals 5, Reykjavik Iceland
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA