VasoView HemoPro Harvesting Systems Recalled for Silicone Detachment Risk

What You Should Do

1. This recall involves VasoView HemoPro Endoscopic Vessel Harvesting Systems with product codes VH-3000-W and VH-3500.
2. Identify if your device is affected by checking the product code and lot number found on the device's labeling or packaging. See the Affected Products section below for the full list of affected codes.
3. Stop using the recalled harvesting systems immediately to prevent potential patient injury or device failure during surgical procedures.
4. Contact Maquet Cardiovascular, LLC or your medical supply distributor to arrange for the return, replacement, or correction of any affected units in your inventory.
5. Refer to the urgent medical device recall letter sent by Maquet Cardiovascular on September 20, 2024, for specific handling and return instructions.
6. For additional questions or to report a safety concern, call the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

Affected Products