Maquet Cardiovascular, LLC 2024-07-17 Health serious FDA
Health · FDA · Recall #FDA-Z-2337-2024
The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in… Recall
Issued July 17, 2024 · Maquet Cardiovascular, LLC
In July 2024, Maquet Cardiovascular, LLC recalled the The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
There were 27 complaints between March 22, 2024, and April 30, 2024, related to VH-3500 and VH-4000, reporting that the C-Ring wire was straightened (due to insufficient bend radius) and that the distance between C-Ring and Harvesting Tool was closer than normal. No adverse events have been reported to date in direct association with this issue.
What you should do
- 1 Stop using The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in… 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 17, 2024
- Units affected
- Not reported
- Sold at
- NationwideForeign: AT DE DK ES GB HK IT NL ZA
- Recall number
- FDA-Z-2337-2024
- 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.