CLASS II ONGOING Device recall · Reported 23 Apr 2025 · FDA Enforcement Report

Maquet VH-3010 Power Supply recalled by Maquet Cardiovascular

Maquet Cardiovascular is recalling Maquet VH-3010 Power Supply, distributed nationwide in the US. The recall was initiated on 10 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel No. VH-3010; UDI-DI: 0060756770826; Serial No. 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, H24080055G, H24080025G, H24080052G, H24080048G, H24080093G, H24080126G, H24080073G, H24080007G, H23060082G, H24080075G, H24080113G, H24080127G, H24080011G, H24080005G, H24080013G, H24080023G, H24080057G, H24080110G, H24080009G, H24080067G, H24080029G, H24080043G, H24080183G, H24080165G, H24080017G, H24080001G, H24080037G, H24080060G, H24080072G, H24080076G, H24080045G, H24080024G, H24080028G, H24080114G, H24080136G, H24080062G, H24080018G, H24080054G, H24080063G, H24080112G, H24080118G, H24080071G, H24080182G, H24080002G, H24080004G, H24080014G, H24080019G, H24080021G, H24080035G, H24080036G, H24080039G, H24080046G, H24080050G, H24080059G, H24080081G, H24080082G, H24080083G, H24080125G, H24080186G, H24080189G.

Quantity recalled110 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1577-2025
FDA event ID: 96392
Recalling firm: Maquet Cardiovascular, Wayne, NJ
Classification: Class II
Status: Ongoing
Recall initiated: 10 Mar 2025
FDA classified: 16 Apr 2025
Reported: 23 Apr 2025
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

10 Mar 2025	Recall initiated by company
16 Apr 2025	Classified by FDA	+37 days
23 Apr 2025	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.

Product as listed by the FDA

Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).

Where it was distributed

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, United Kingdom, United States.

Nationwide 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

Stores named: Walmart

Questions about this recall

Is Maquet VH-3010 Power Supply recalled?

Yes. Maquet Cardiovascular recalled Maquet VH-3010 Power Supply on 10 Mar 2025. The recall is Class II and its status is Ongoing. Recall number Z-1577-2025.

Why was it recalled?

Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.

Which lots are affected?

Model No. VH-3010; UDI-DI: 0060756770826; Serial No. 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, H24080055G, H24080025G, H24080052G, H24080048G, H24080093G, H24080126G, H24080073G, H24080007G, H23060082G, H24080075G, H24080113G, H24080127G, H24080011G, H24080005G, H24080013G, H24080023G, H24080057G, H24080110G, H24080009G, H24080067G, H24080029G, H24080043G, H24080183G, H24080165G, H24080017G, H24080001G, H24080037G, H24080060G, H24080072G, H24080076G, H24080045G, H24080024G, H24080028G, H24080114G, H24080136G, H24080062G, H24080018G, H24080054G, H24080063G, H24080112G, H24080118G, H24080071G, H24080182G, H24080002G, H24080004G, H24080014G, H24080019G, H24080021G, H24080035G, H24080036G, H24080039G, H24080046G, H24080050G, H24080059G, H24080081G, H24080082G, H24080083G, H24080125G, H24080186G, H24080189G.

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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