Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, o
Summary
The FDA issued a Class II for Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printe by Maquet Cardiovascular, LLC. Reason: Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device..
Details
Source
Device Recall
External ID
Z-0210-2024
Action Date
2023-11-08
Status
Ongoing
Category
device
Product Description
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).
Lot/Code Info: UDI-DI: 00607567700239, Lot: 3000313857.
Quantity Affected: N/A
Reason for Recall
Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.
Distribution
US (AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX) and Canada.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-19
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 156 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-0210-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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