Maquet recalls VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System due to C-Ring wire straightening causing improper device positioning. 27 complaints reported between March 22 and April 30, 2024.
There were 27 complaints between March 22, 2024, and April 30, 2024, related to VH-3500 and VH-4000, reporting that the C-Ring wire was straightened (due to insufficient bend radius) and that the distance between C-Ring and Harvesting Tool was closer than normal. No adverse events have been reported to date in direct association with this issue.
Maquet is recalling the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System after 27 complaints reported that the C-Ring wire became straightened, making the device less effective. This could lead to improper positioning during surgery, though no injuries have been reported.
The C-Ring wire can become straightened due to insufficient bend radius, causing the distance between the C-Ring and Harvesting Tool to be closer than normal. This may lead to improper positioning during endoscopic vessel harvesting procedures.
Surgical teams using the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System with specific lot numbers. Patients undergoing vascular surgery are most at risk if the device is used incorrectly.
Check for lot numbers: 3000371260, 3000378288, 3000372477, 3000378950, 3000376542, 3000380314, 3000377320, 3000380847, 3000371798, 3000378554. The device is designed for use with the 7 mm Extended Length Endoscope.
Identify the lot number on the device packaging or label to confirm if it is affected.
No adverse events have been reported to date, but 27 complaints indicate the C-Ring wire may become straightened, potentially causing improper device positioning during surgery.
The recall does not specify a remedy, so contact Maquet directly for guidance on whether to continue using the device.
Check the lot number on the device packaging or label; affected devices have specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-2338-2024 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-2338-2024 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
