VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500
Summary
The FDA issued a Class II for VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500 by Maquet Cardiovascular, LLC. Reason: Some batches of product were not sterilized to their minimum sterilization specification..
Details
Source
Device Recall
External ID
Z-1335-2023
Action Date
2023-04-12
Status
Ongoing
Category
device
Product Description
VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500
Lot/Code Info: UDI-DI: 00607567701250; Lot Numbers: 3000280189, 3000276183
Quantity Affected: 900 units
Reason for Recall
Some batches of product were not sterilized to their minimum sterilization specification.
Distribution
Worldwide distribution - US Nationwide and the countries of Brazil, China.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-06
Company
Wayne, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 130 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Maquet Cardiovascular, LLC has 41 FDA actions in our database, including 37 recalls and 4 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Maquet Cardiovascular, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Maquet Cardiovascular, LLC have FDA actions?
Maquet Cardiovascular, LLC has 41 FDA actions in our database, including 37 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1335-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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