VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W
Reported: April 12, 2023 Initiated: March 6, 2023 #Z-1337-2023
Product Description
VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W
Reason for Recall
Some batches of product were not sterilized to their minimum sterilization specification.
Details
- Recalling Firm
- Maquet Cardiovascular, LLC
- Units Affected
- 235 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Brazil, China.
- Location
- Wayne, NJ
Frequently Asked Questions
What product was recalled? ▼
VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W. Recalled by Maquet Cardiovascular, LLC. Units affected: 235 units.
Why was this product recalled? ▼
Some batches of product were not sterilized to their minimum sterilization specification.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 12, 2023. Severity: Moderate. Recall number: Z-1337-2023.
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