The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended ... — FDA record Z-2176-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 17, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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.
Reason
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.
Classification
Class II
Recalling firm
Maquet Cardiovascular, LLC
Quantity
37,186 units
Agency-reported status
Ongoing
Source record identifier
Z-2176-2024

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What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityModel 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.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide distribution - US Nationwide and the countries of Australia Brazil, Canada, China, EEA, India, Korea, New Zealand, Southern Africa, Taiwan, Thailand, Turkey, & United Kingdom.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jul 3, 2024
Recall initiation date
May 17, 2024
Center classification date
Jun 24, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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