Maquet Cardiovascular, LLC 2024-01-24 Health serious FDA
Health · FDA · Recall #FDA-Z-0723-2024
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . Recall
Issued January 24, 2024 · Maquet Cardiovascular, LLC
In January 2024, Maquet Cardiovascular, LLC recalled the Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W ., a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arterial conduit for patients undergoing a coronary artery bypass graft (CABG) or peripheral bypass graft surgery.
What you should do
- 1 Stop using Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . 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
- January 24, 2024
- Units affected
- Not reported
- Sold at
- US: OUS: China, Brazil, Hong Kong.
- Recall number
- FDA-Z-0723-2024
- 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.