Vasoview Hemopro recall
VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W
Why was Vasoview Hemopro recalled?
Some batches of product were not sterilized to their minimum sterilization specification.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 00607567700345; Lot Numbers: 3000274687
- Product
- VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W
- Recalling firm
- Maquet Cardiovascular, LLC
- Quantity
- 235 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Brazil, China.
- Recall date
- April 12, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)