Maquet Cardiovascular, LLC 2024-07-03 Health serious FDA
Health · FDA · Recall #FDA-Z-2175-2024
The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1.… Recall
Issued July 3, 2024 · Maquet Cardiovascular, LLC
In July 2024, Maquet Cardiovascular, LLC recalled the The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1.…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for there to be a fluid ingress into the handle of the harvesting tool, which may lead to the device not providing cautery or providing cautery when not intended.
What you should do
- 1 Stop using The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1.… 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
- July 3, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Australia Brazil, Canada, China, EEA, India, Korea, New Zealand, Southern Africa
- Recall number
- FDA-Z-2175-2024
- 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.