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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

Vasoview Hemopro 3 Harvesting Systems Recalled for Mechanical Defects

Agency Publication Date: September 25, 2025
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Summary

Maquet Cardiovascular, LLC has recalled 98 units of the Vasoview Hemopro 3 Endoscopic Vessel Harvesting (EVH) System, Model No. C-VH-6000. These surgical kits, used by healthcare professionals to harvest blood vessels, were found to have defects when removed from their packaging during the initial launch phase. Reported issues include bent tips at the jaw attachment site, jaws that do not close completely, and heater wires that have pulled away from the tool's jaws.

Risk

A defective harvesting tool could fail to properly cut or cauterize blood vessels during surgery, potentially leading to patient bleeding or the need for additional surgical intervention. While these defects were discovered 'out-of-box' before use, they pose a risk if the device is used in a clinical setting.

What You Should Do

  1. This recall affects the Vasoview Hemopro 3 Endoscopic Vessel Harvesting (EVH) System, specifically Model No. C-VH-6000.
  2. Identify affected products by checking for lot numbers 3000486429, 3000487231, 3000487726, or 3000488639 and UDI 00607567701274 on the device packaging.
  3. Stop using the recalled device immediately and remove it from surgical inventory.
  4. Contact Maquet Cardiovascular, LLC or your medical equipment distributor to arrange for the return, replacement, or correction of the affected units.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding medical device recalls.

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: Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000, VH-6001, and VH-6010)
Model / REF:
C-VH-6000
VH-6000
VH-6001
VH-6010
Lot Numbers:
3000486429
3000487231
3000487726
3000488639
UDI:
00607567701274

Failure modes include angled deformity at the jaw attachment, jaws not fully closed out-of-box, and heater wire lifted/flexed away from jaws.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97469
Status: Active
Manufacturer: Maquet Cardiovascular, LLC
Sold By: Medical distributors; Surgical centers; Hospitals
Manufactured In: United States
Units Affected: 98 units
Distributed To: Florida, Illinois, Maryland, Texas
Agency Last Updated: November 14, 2025

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.