Maquet VasoView HemoPro Endoscopic Vessel Harvesting System Recall: Silicone Detachment
Maquet recalls VasoView HemoPro Endoscopic Vessel Harvesting System (product codes VH-3000-W and VH-3500) due to reports of silicone detaching from the Harvesting Tool during use. Affected units have specific lot numbers and product codes.
Lower-risk recall
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
Contact the company
What happened, in plain English
Maquet is recalling its VasoView HemoPro Endoscopic Vessel Harvesting System (product codes VH-3000-W and VH-3500) because silicone parts have been reported to detach from the Harvesting Tool during use. This could lead to potential injury if the detached part causes a blockage or other complications during medical procedures. Read more at govinfonow.com/recall/53898-maquet-vasoview-hemopro-endoscopic-vessel-harvesting-system-recall-silicone-detachment.
Source Summary by GovInfoNow · govinfonow.com/recall/53898-maquet-vasoview-hemopro-endoscopic-vessel-harvesting-system-recall-silicone-detachment · Updated September 23, 2026 · FDA enforcement record: FDA #Z-0092-2025
Cite this page
“Maquet VasoView HemoPro Endoscopic Vessel Harvesting System Recall: Silicone Detachment.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/53898-maquet-vasoview-hemopro-endoscopic-vessel-harvesting-system-recall-silicone-detachment. Based on FDA recall #Z-0092-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0092-2025%22&limit=1).
Why it’s dangerous
Silicone parts can detach from the Harvesting Tool during medical procedures, potentially causing blockages or other complications. This issue has been reported but does not indicate a high risk of serious injury in normal use.
Who’s affected
Medical professionals using the VasoView HemoPro Endoscopic Vessel Harvesting System for procedures. Patients undergoing surgeries with this device may be at risk if the silicone detaches during use.
How to tell if you have this one
Check for product codes VH-3000-W or VH-3500 with specific lot numbers listed in the recall notice. The device is used in medical procedures for vessel harvesting.
- Brand
Maquet- Category
Medical device
What to do — step by step
Check Product Details
Review the product code and lot number on your device to confirm if it is affected by this recall.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 47 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-0092-2025 (September 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0092-2025 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.