VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
Reported: November 6, 2024 Initiated: September 20, 2024 #Z-0092-2025
Product Description
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
Reason for Recall
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
Details
- Recalling Firm
- Maquet Cardiovascular, LLC
- Units Affected
- 28,809 units
- Distribution
- Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.
- Location
- Wayne, NJ
Frequently Asked Questions
What product was recalled? ▼
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500. Recalled by Maquet Cardiovascular, LLC. Units affected: 28,809 units.
Why was this product recalled? ▼
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 6, 2024. Severity: Critical. Recall number: Z-0092-2025.
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