Events

Retiro De Equipo (Recall) de Device Recall Pentacam AXL

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 Oculus Optikgeraete GMBH.

¿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
    78606
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0635-2018
  • Fecha de inicio del evento
    2017-11-21
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2018-03-22
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=159872
  • 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
    Device,analysis,anterior segment - Product Code MXK
  • Causa
    The device software versions have an anomaly which may produce an erroneous marking for the quality specification value.
  • Acción
    Oculus issued an email on November 21, 2017 to their U.S. subsidiary which contained a Mandatory Software Update notification. The email informed the U.S. subsidiary that a mandatory software update was planned for the Pentacam AXL in possession of their customers, provided the software versions affected, and the reason for the mandatory update. The email explained the USB thumb drive will be shipped to the U.S. subsidiary for each serial number that may be affected. The U.S. subsidiary was to match the serial numbers to their customers and complete the attached customer letter for issuance to each of the customers. The U.S. subsidiary is then supposed to issue the letter and the USB thumb drive via certified mail to each of their customers who have the affected serial numbers. The customer is to send back the completed, signed form verifying the mandatory software update has been installed on all working places on which the Pentacam AXL software is running or that the procedure was performed by an authorized distributor. For further questions, please call (425) 670-9977

Device

Device Recall Pentacam AXL
  • Modelo / Serial
    Serial numbers:  70100 0021 6190, 70100 0301 5170, 70100 0311 6150, 70100 0331 7130, 70100 0401 5101, 70100 0421 6101, 70100 0641 7170, 70100 0831 7150, 70100 1021 6190, 70100 1101 5170, 70100 1541 7170, 70100 1631 7140, 70100 1731 7140, 70100 1831 7150, 70100 1901 6130, 70100 2211 6150, 70100 2221 6190, 70100 2231 7130, 70100 2241 7160, 70100 2511 6170, 70100 2641 7170, 70100 2731 7140, 70100 2801 6130, 70100 2821 7110, 70100 2931 7150, 70100 3221 6190, 70100 3701 6110, 70100 3731 7140, 70100 3931 7150, 70100 4041 7160, 70100 4211 6150, 70100 4231 7130, 70100 4401 5121, 70100 4511 6170, 70100 4711 6170, 70100 4831 7150, 70100 4931 7150, 70100 5311 6160, 70100 5531 7140, 70100 5611 6170, 70100 5621 6111, 70100 5831 7150, 70100 5931 7150, 70100 6101 5170, 70100 6221 6101, 70100 6231 7130, 70100 6331 7130, 70100 6401 5121, 70100 6421 6101, 70100 6631 7140, 70100 6801 6130, 70100 6811 6190, 70100 6821 7110, 70100 7041 7160, 70100 7221 6101, 70100 7401 5121, 70100 7511 6170, 70100 7531 7140, 70100 7631 7140, 70100 7731 7150, 70100 7831 7150, 70100 7931 7150, 70100 8121 6190, 70100 8141 7160, 70100 8511 6170, 70100 8531 7140, 70100 8611 6170, 70100 8631 7140, 70100 8721 7110, 70100 8731 7150, 70100 9041 7160, 70100 9221 6101, 70100 9231 7130, 70100 9301 5101, 70100 9411 6160, 70100 9521 6111, 70100 9711 6190, 70100 9731 7150, 70100 9911 6190, 70100 9931 7150, 70100 7411 6160, 70100 8021 6190, and 70100 4531 7140.
  • Clasificación del producto
    Ophthalmic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Distribution to the states of : CA and FL. There were no foreign/military/government accounts.
  • Descripción del producto
    OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13. The firm name on the label is OCULUS Optikgerate GmbH, Made in Germany. || The Pentacam AXL is designed to take photos of the anterior segment of the eye, which includes the cornea, pupil, anterior chamber, and lens of the eye, to evaluate corneal shape, analyze condition of the lens (opaque crystalline lens), analyze the anterior chamber angle, analyze anterior chamber depth, analyze the volume of the anterior chamber, analyze anterior or posterior cortical opacity, analyze the location of cataracts (nuclear, sub capsular and/or cortical), using cross slit imaging with densitometry, corneal thickness, axial length, and white-to-white distance. The Pentacam AXL also performs calculations to assist physicians in determining the power of the intraocular lens for implantation.
  • Manufacturer
    Oculus Optikgeraete GMBH

Manufacturer

Oculus Optikgeraete GMBH
  • Dirección del fabricante
    Oculus Optikgeraete GMBH, Munchholzhauser Str. 29, Wetzlar Germany
  • Source
    USFDA