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FDAFDA · Alimentos y medicamentos·N.º oficial Z-0959-2019

BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic visualization of the heart, blood vessels or lymphatic system during or after injection of a contrast medium. It is to be used in the diagnosis of the circulatory vascular system while being combined with a positioning device and other devices.

Publicado el 6 de marzo de 2019 · Inicio del retiro: 14 de enero de 2019

Estado reportado al momento de publicación: Terminated — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.

Qué peligro representa

Normal operation of the device is to power up the device in the morning, register the first patient, and then perform a fluoroscopy. If, however, the user powers up the device in the morning and makes an error by starting a fluoroscopy while the first patient is still being registered, the device application will abnormally terminate and require service intervention before it can be used again. This event will not occur after the first patient procedure.

Qué hacer

Voluntary: Firm initiated · E-Mail

Detalles del retiro

Fabricante
Shimadzu Medical Systems Usa Com
Distribuidor
US Nationwide Distribution in the states of IN, OH, IL, SC
Lote
Serial Numbers: 40AD58C4B001, 40AD58C55001, 0261Q80503, 0261Q80804, 0161Q84501, 0161Q83102, 3M7A16A1A001, 0161Q82302
Clasificación de riesgo
Class II
Área (FDA)
device
País
United States

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