Events

Retiro De Equipo (Recall) de Device Recall Customed

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 Customed, 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
    Recall
  • ID del evento
    68536
  • Clase de Riesgo del Evento
    Class 1
  • Número del evento
    Z-2338-2014
  • Fecha de inicio del evento
    2014-05-20
  • Fecha de publicación del evento
    2014-08-29
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2017-08-14
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=129232
  • 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
    laparoscopy kit - Product Code FWZ
  • Causa
    Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). this could result in an injury to the patient due to product contamination or loss of sterility condition.
  • Acción
    Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit. Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540

Device

Device Recall Customed
  • Modelo / Serial
    Product code 900-620, 28 lots: 111113132 111123276 112010192 112020517 112030733 112041340 112052000 112062500 112072808 112083437 112093729 112114579 112124875 113015455 113025964 113036374 113036444 113068176 113088879 113099447 113109862 131210833 140111241 140211733 140211943 140412839 140513377 140513456
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.
  • Descripción del producto
    ARTHROSCOPY PACK - || (1) MAYO STAND COVER REINFORCED LIF || (1 0) GAUZE SPONGES 4" X 4" 16PL Y || (1) TUBE SUCTION CONNECTING X" X 12' LIF || (1) IMP. STOCKINETTE || (1) SURGICAL BLADE #11 STAINLESS STEEL || (1) ANESTHESIA SPINAL NEEDLE 18G X 3 ~ || (1) SYRINGE Sec WITH NEEDLE 21G X 1 ~ LUER LOCK LIF || (2) ELASTIC BANDAGE 6" X 5yrd LIF || (1) TUR Y SET 81 "2.1m REGULAR CLAM || (2) NEEDLE HYPODERMIC 18G X 1 ~ || (1) TABLE COVER 50" X 90" REINFORCED LIF || (5) TOWEL ABSORBENT 15" X 20" LIF || (2) DRAPE UTILITY WITH TAPE LIF || (1) DURAPREP SURGICAL SOLUTION 26m I LIF || (1) U-DRAPE 60" X 70" WITH TAPE SPLIT || (1) Pr. NEUTRALON SURGEON GLOVES #7.5 || (1) Pr. NEUTRALON SURGEON GLOVES #8 || (1) Pr. NEUTRALON SURGEON GLOVES #8.5 || (2) GOWN IMPERVIOUS REINFORCED X-LARGE SMS || (10) GAUZE SPONGES 4" X 4" 16PLY XRD || (2) STRIPS TAPE || (1) SHEET ARTHROSCOPY T STD SMS WITH POUCH LIF || (1) DRAPE VIDEO CAMERA LIF || EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
  • Manufacturer
    Customed, Inc

Manufacturer

Customed, Inc
  • Dirección del fabricante
    Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
  • Empresa matriz del fabricante (2017)
    Customed Inc
  • Source
    USFDA