Maquet Cardiovascular, LLC 2024-11-06 Health critical FDA
Health · FDA · Recall #FDA-Z-0092-2025
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500 Recall
Issued November 6, 2024 · Maquet Cardiovascular, LLC
In November 2024, Maquet Cardiovascular, LLC recalled the VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
What you should do
- 1 Stop using VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Maquet Cardiovascular, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Maquet Cardiovascular, LLC
- Category
- Health
- Recall date
- November 6, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.
- Recall number
- FDA-Z-0092-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Maquet Cardiovascular, LLC has 7 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.