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-2313-2014
  • 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=129146
  • 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
    Angiography/angioplasty kit - Product Code OEQ
  • 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 900-210, 30 lots: 112030717 112041290 112041446 112051934 112072622 112093725 112114388 112114598 113015442 113015630 113036436 113036760 113047216 113057458 113057699 113057816 113068045 113068165 113078572 113089023 113099285 113109786 131110235 131110605 131210967 140111414 140211876 140312332 140412833 140513348
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿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
    ANGIOGRAPHY PACK- - || (4) CLOTH HUCK TOWEL BLUE UF || (1) TABLE COVER REINFORCED 50" X 90" LIF || (1) SYRINGE 20cc WITHOUT NEEDLE LUER LOCK UF || (2) MEDICINE CUP 2oz. LIF || (3) UTILITY BOWL 32oz UF || (1) EMESIS BASIN 10 IN 700cc || (4) TOWEL CLAMP || (3) ABSORBENT TOWELS 15" X 20" LIF || (1) SYRINGE 3cc WITHOUT NEEDLE LUER LOCK L/F || (1) HALSTED MOSQUITO || (1) PVP SCRUB 8" STICK SPONGE || (1) TRAY PLATFORM LARGE || (3) LABELS FOR SKIN MARKERR || (1) LABEL FOR MEDICATION SALINE NORMAL BLUE || (1) LABEL FOR MEDICATION TRIDIL VIOLETA || (1) NEEDLE HYPODERMIC 18G X 1 'h || (4) SYRINGE 10ccWITHOUT NEEDLE LUER LOCK LIF || (1) SYRINGE 30cc WITHOUT NEEDLE LUER LOCK LIF || (2) UTILITY BOWL 16oz || (3) BAND BAG WITH RUBBAND & TAPE LIF || (25) GAUZE SPONGE 4" X 4" 16PL Y XRD LIF || (1) DRAPE ANGlO 75" X 145" || (1) NEEDLE HYPODERMIC 21 G X 1 'h LIF || (1) SAFETY SCALPEL #11 LIF || (1) GOWN STANDARD SMS LARGE VELCRO NECK || (2) NEEDLE HYPODERMIC 23G X 1" || (1) TRAY ORGANIZER FULL DEEP || (1) GOWN LARGE NON REINFORCED SMS TOWEL & WRAP || (1) LABEL XYLOCAINE FOR MEDICATION YELLOW || (1) LABEL CONTRASTE FOR MEDICATION GREEN || (1) LABEL FOR MEDICATION INTEGRILIN RED || (1) PVP PAINT 8" STICK SPONGE || 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