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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Maquet VH-3010 Power Supply Recalled for Potential Heating Failure

Agency Publication Date: April 16, 2025
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Summary

Maquet Cardiovascular, LLC is recalling approximately 110 units of the Maquet VH-3010 Power Supply, which provides power to the harvesting tool in the Vasoview Hemopro EVH System (HemoPro 2). The recall is due to the use of an incorrect resistor in the power supply, which can prevent the jaws of the HemoPro 2 tool from heating up adequately during surgery. No incidents or injuries have been reported to date regarding this issue.

Risk

If the power supply does not deliver adequate heat to the surgical tool, the device may fail to perform correctly during endoscopic vessel harvesting procedures. This can lead to procedural delays or the need for alternative medical equipment, which could impact patient care.

What You Should Do

  1. This recall affects the Maquet VH-3010 Power Supply used to deliver power to the HemoPro 2 tool within the Vasoview Hemopro EVH System.
  2. Identify the affected power supplies by checking for Model No. VH-3010 and UDI-DI 0060756770826 on the device label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device immediately.
  4. Contact Maquet Cardiovascular, LLC or your authorized medical distributor to arrange for a return, replacement, or correction of the power supply unit.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions or to report any adverse events related to this product.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Maquet VH-3010 Power Supply (Vasoview Hemopro EVH System)
Model / REF:
VH-3010
Serial Numbers (110):
H24080065G
H24080074G
H24080012G
H24080022G
H24080184G
H24080185G
H24080051G
H24080117G
H24080069G
H24080016G
H24080079G
H24080041G
H24080056G
H24080030G
H24080068G
H24080034G
H24080058G
H24080026G
H24080033G
H24080020G
H24080032G
H24080053G
H24080066G
H24080077G
H24080144G
H24080123G
H24080042G
H24080070G
H24080008G
H24080003G
H24080174G
H24080064G
H24080027G
H24080044G
H24080047G
H24080049G
H24080061G
H24080078G
H24080010G
H24080138G
H24080080G
H24080006G
H24080015G
H24080038G
H24080085G
H24080084G
H24080031G
H24080101G
H24080148G
H24080040G
UDI:
0060756770826

Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96392
Status: Active
Manufacturer: Maquet Cardiovascular, LLC
Sold By: Authorized medical distributors
Manufactured In: United States
Units Affected: 110 units
Distributed To: Alabama, California, Colorado, District of Columbia, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Maryland, Michigan, Minnesota, Missouri, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, Texas, Utah, Virginia, Wisconsin, West Virginia
Agency Last Updated: January 12, 2026

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.