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Preguntas frecuentes
Créditos
Devices
Device Recall RadSuite software
Modelo / Serial
This potential patient safety issue is only present in the following versions when a reverse workflow is used: 2004-R6.x, 5.10.x, 5.20, 5.25, 5.30.1, 5.30.2, 5.30.2 SB0344, 5.30.3, 5.30.4, 5.30.4 HF0418E, 5.30.5, 5.30.5 HF0404E, 5.30.5 HF0413E, 5.30.5 HF390E, 5.30.5 SB0368, 5.30.6, 5.30.6 HF0405E, 5.30.6 HF0406E, 5.30.7, 5.30.7 HF0429E, 5.30.7 HF0441E, 5.30.7 HF0446E, 5.30.7 HF0470E, 5.30.7 HF0473E, 5.30.8, 5.30.8 HF0477E, 5.30.8 HF0490E, 5.30.8 HF0495 SB0508E, 5.30.8 HF0495E, 5.30.8 HF0495E SB504E, 5.30.8 HF0550, 5.30.8 SB0485E, 5.30.8 SB0486E, 5.30.X SB0381E, 5.35.1, 5.35.1 HF0487E, 5.35.1 HF0489E, 5.35.2, 5.35.3, 5.35.4, 5.35.4 HF0513, 5.35.4 HF0518, 5.35.4 HF0528, 5.35.4 HF0531, 5.35.4 HF0535, 5.35.4 HF0546, 8.30.0. NOTE: The standard workflow is not impacted. .
Clasificación del producto
Radiology Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Distribution was nationwide to medical facilities. Government distribution was made to LA and OK.
Descripción del producto
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Manufacturer
Merge Healthcare, Inc.
1 Event
Retiro De Equipo (Recall) de Device Recall RadSuite software
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Fabricante
Merge Healthcare, Inc.
Dirección del fabricante
Merge Healthcare, Inc., 900 Walnut Ridge Dr, Hartland WI 53029-8347
Empresa matriz del fabricante (2017)
International Business Machines Corp.
Source
USFDA
Language
English
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