Maquet VH-3010 Power Supply Recall: Incorrect Resistor May Cause HemoPro 2 Heating Failure
Maquet recalls VH-3010 Power Supply units that may cause HemoPro 2 harvesting tool to fail to heat properly due to incorrect resistor use. Affected units have specific serial numbers.
Lower-risk recall
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
Contact the company
What happened, in plain English
Maquet is recalling its VH-3010 Power Supply units because they may have an incorrect resistor that prevents the HemoPro 2 harvesting tool from heating properly. This could lead to inadequate tissue processing during medical procedures. Read more at govinfonow.com/recall/52651-maquet-vh-3010-power-supply-recall-incorrect-resistor-may-cause.
Source Summary by GovInfoNow · govinfonow.com/recall/52651-maquet-vh-3010-power-supply-recall-incorrect-resistor-may-cause · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1577-2025
Cite this page
“Maquet VH-3010 Power Supply Recall: Incorrect Resistor May Cause HemoPro 2 Heating Failure.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52651-maquet-vh-3010-power-supply-recall-incorrect-resistor-may-cause. Based on FDA recall #Z-1577-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1577-2025%22&limit=1).
Why it’s dangerous
The power supply uses an incorrect resistor that may prevent the HemoPro 2 harvesting tool from heating tissue adequately. This could result in incomplete tissue processing during medical procedures but does not pose an immediate risk of injury.
Who’s affected
Medical professionals using the HemoPro 2 system with the recalled VH-3010 power supply. The risk is low as the hazard involves heating failure rather than immediate injury.
How to tell if you have this one
Check for the model number VH-3010 and serial numbers listed in the recall notice (e.g., H24080065G, H24080074G). The power supply is used with the Vasoview Hemopro EVH System (HemoPro 2).
- Brand
Maquet- Category
Medical device
What to do — step by step
Check Power Supply Model
Verify your power supply has model number VH-3010 and one of the listed serial numbers.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 25 states.
FDA distribution: “Worldwide - US Nationwide distribution in the states of AL, CA, CO, DC, FL, GA, IA, ID, IL, IN, KY, MD, MI, MN, MO, NC, NH, NJ, NY, OH, PA, PR, TX, UT, VA, WI, WV and the countries of China, Japan, Netherlands, New Zealand, Singapore,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, California, Colorado, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Maryland, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Puerto Rico, Texas, Utah, Virginia, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 44 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1577-2025 (March 10, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1577-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.