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FDAFDA · Alimentos y medicamentos·N.º oficial Z-2176-2024

The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches. The harvesting tool has two curved jaws. One of the jaws contains the heating elements for branch cutting and cauterization and spot cautery. An area near the tip of the convex side of the jaw is used for spot cautery. The activation toggle is used to control the jaws to activate the heating elements. Positioning of the device, cutting, and cauterization are performed under endoscopic visualization.

Publicado el 3 de julio de 2024 · Inicio del retiro: 17 de mayo de 2024

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

Qué peligro representa

Potential for there to be a fluid ingress into the handle of the harvesting tool, which may lead to the device not providing cautery or providing cautery when not intended.

Qué hacer

Voluntary: Firm initiated · Letter

Detalles del retiro

Fabricante
Maquet Cardiovascular, LLC
Distribuidor
Worldwide distribution - US Nationwide and the countries of Australia Brazil, Canada, China, EEA, India, Korea, New Zealand, Southern Africa, Taiwan, Thailand, Turkey, & United Kingdom.
Lote
Model No. VH-3500, VH-3000-W; UDI: 00607567701250, 00607567700345; Lot No. 3000314373, 3000314821, 3000316023, 3000316024, 3000316027, 3000317501, 3000317575, 3000317576, 3000318302, 3000318901, 3000320140, 3000320141, 3000320773, 3000321483, 3000321723, 3000323214, 3000324397, 3000324409, 3000325013, 3000325249, 3000325689, 3000325776, 3000328206, 3000328561, 3000328562, 3000329723, 3000330445, 3000331131, 3000331388, 3000332428, 3000332510, 3000332993, 3000333524, 3000333829, 3000333956, 3000333967, 3000334315, 3000335670, 3000336708, 3000337272, 3000339701, 3000340534, 3000341133, 3000341675, 3000342250, 3000342251, 3000343264, 3000343266, 3000344887, 3000351187, 3000352770, 3000354226, 3000354228, 3000355224, 3000355369, 3000355798, 3000356048, 3000357837, 3000360574, 3000360576, 3000360775, 3000361036, 3000361423, 3000361707, 3000362064, 3000362258, 3000362671, 3000362933, 3000363162, 3000363947, 3000364082, 3000364309, 3000364520, 3000365379, 3000365391, 3000366446, 3000366831, 3000367160, 3000367439, 3000367542, 3000367852, 3000368165, 3000368658, 3000369005, 3000369122, 3000369645, 3000370069, 3000370290, 3000372257, 3000375534, 3000375776, 3000376132, 3000376388, 3000376542, 3000376883, 3000376883, 3000377320, 3000377699, 3000378079, 3000378654, 3000379282, 3000379691, 3000380264, 3000380475, 3000380671, 3000381287, 3000381620, 3000382054, 3000383367, 3000383779, 3000384088, 3000388588.
Clasificación de riesgo
Class II
Área (FDA)
device
País
United States

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