Maquet Vasoview 6 Pro: Incorrect Box Artwork May Cause Confusion
Maquet recalls Vasoview 6 Pro (VV6) endoscopic vessel harvesting system with incorrect box artwork that could lead to confusion about the device model.
Lower-risk recall
Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.
Contact the company
What happened, in plain English
Maquet is recalling Vasov:6 Pro (VV6) endoscopic vessel harvesting systems with incorrect box artwork that might cause confusion about the device model. This could lead to using the wrong device in medical procedures. Read more at govinfonow.com/recall/57304-maquet-vasoview-6-pro-incorrect-box-artwork-may-cause-confusion.
Source Summary by GovInfoNow · govinfonow.com/recall/57304-maquet-vasoview-6-pro-incorrect-box-artwork-may-cause-confusion · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0210-2024
Cite this page
“Maquet Vasoview 6 Pro: Incorrect Box Artwork May Cause Confusion.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57304-maquet-vasoview-6-pro-incorrect-box-artwork-may-cause-confusion. Based on FDA recall #Z-0210-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0210-2024%22&limit=1).
Why it’s dangerous
The device comes in a box with artwork for a different model (Vasoview Hemopro 2). This could cause confusion during medical procedures if the wrong device is used.
Who’s affected
Medical professionals who use the Vasoview 6 Pro system may be affected if they receive the device with incorrect box artwork. Those most at risk are healthcare providers handling the recalled units.
How to tell if you have this one
Check for the model VH-2400 printed on the outer label, inner label, and instructions. The box may show artwork for Vasoview Hemopro 2 instead of Vasoview 6 Pro.
- Brand
Maquet Cardiovascular- Category
Medical device
What to do — step by step
Check Box Artwork
Look for artwork showing Vasoview Hemopro 2 on the box instead of Vasoview 6 Pro.
Where it went and when
Where it was distributed
Distributed in 13 states, and outside the U.S.
FDA distribution: “US (AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX) and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, California, Florida, Georgia, Indiana, Kentucky, Michigan, New Jersey, Oklahoma, Pennsylvania, Tennessee, Texas.
Recall timeline
FDA published this recall 50 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0210-2024 (September 19, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0210-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.