Events

Retiro De Equipo (Recall) de Male, 16Fr, Straighttip Intermittent Urinary Catheters M16

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 Cure Medical LLC.

¿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
    63241
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0004-2013
  • Fecha de inicio del evento
    2012-09-19
  • Fecha de publicación del evento
    2012-10-02
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2013-02-07
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=113089
  • 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
    Catheter, straight - Product Code EZD
  • Causa
    The firm initiated the product recall because labeling on some of the intermediate boxes of catheters identify the contents to be m16c, a coud¿-tip catheters while the actual contents are m16fr male, 16fr, straight-tip catheters with the pouch and the case box labeled as m16fr male, 16fr, straight-tip catheters.
  • Acción
    Cure Medical LLC sent an Urgent Medical Device Correction and Removal Notification letter dated September 19, 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. The letter instructed the customers to: a) Check their shelves for M16C with lot number 120425 and quarantine all affected product. b) Verify the contents (pouch label) are M16C and correspond with the intermediate box label. c) If all match, have the dealer sign and return a supplied verification record. d) If any mismatch is found, contact Cure Medical for assignment of a return goods authorization. e) Cure Medical will replace any incorrect product along with processing costs for this situation to the dealer. If affected product was further distributed customers were asked to identify those customers who received them and notify them of the problem. For questions customers were instructed to call 1-800-570-1778.

Device

Male, 16Fr, Straighttip Intermittent Urinary Catheters M16
  • Modelo / Serial
    Total affected product: M16, Lot 120425: 420 cases = 4,200 boxes = 126,000 each. 2017.03 is shown on the product labeling as the expiry date for the product, 4 years and 11 months from the date of packaging. The product, M16, is identified with the following UPC Codes for the individual pouches, intermediate boxes and case labels:  ¿ Pouch Label UPC (M16) = *+M405M16 ¿ Box Label UPC (M16) = *+M405M163I* " Case Label UPC (M16) = *+M405M165K*   Explanation of Lot Number: The lot number represents a planned packaging date of a set of work orders for various products, in the format YYMMDD at the contract manufacturers facility.   At the order planning stage, the packaging date is estimated (based on production cycle time and pre-printed box delivery) and assigned to each work order The lot number represents a planned packaging date of a set of work orders for various products, in the format YYMMDD at the contract manufacturers facility.   At the order planning stage, the packaging date is estimated (based on production cycle time and pre-printed box delivery) and assigned to each work order scheduled for packaging on this estimated date.  Therefore, one lot number may be assigned to multiple catalog numbers. The lot number 120425 was assigned to both M16 and M16C products by the scheduling department  Actual packaging of the M16 occurred from 23 May 2012 through 25 May 2012.  Actual packaging of the M16C occurred from 19 May through 21 May 2012.
  • Clasificación del producto
    Gastroenterology-Urology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in intermediate boxes containing 30 individual, sterile packaged catheters (PA/PE film and dialyzing paper pouches). || There are 30 catheters packaged in sterile pouches that are placed into an intermediate box, 10 of these intermediate boxes packaged into one case. K072539 || The Cure Catheter" device, M16, is an intermittent urinary catheter intended to be used by males for the purpose of bladder drainage. It is manufactured with conventional medical grade, latex-free, biocompatible materials. The straight-tip has been designed to eliminate trauma to the urethra and is provided in 16Fr size in an easy-to-open, sterile, single-use package. The coud¿-tip catheter, M16C, is designed with a curved tip that makes it easier to pass through the curvature of the prostatic urethra in men. It is also used to pass through urethral strictures. This product is prescribed for people who have difficulty or are unable to pass a straight catheter through their urethra and into their bladder.
  • Manufacturer
    Cure Medical LLC

Manufacturer

Cure Medical LLC
  • Dirección del fabricante
    Cure Medical LLC, 2113 Seville Ave, Newport Beach CA 92661-1532
  • Empresa matriz del fabricante (2017)
    Cure Medical Llc
  • Source
    USFDA