VASOVIEW HEMOPRO 3 VH-6010Recalls & reported problems
Maquet Cardiovascular LLC · The Vasoview Hemopro 3 Power Supply is a reusable, AC-powered device intended to be used only with the Vasoview Hemopro 3 Endoscopic Vessel Harvesting System. The device provides DC power output to the Vasoview Hemopro 3 Harvesting Tool to enable cutting and coagulation of vessels and tissue during vessel harvesting procedures. The Vasoview Hemopro 3 Power Supply is positioned outside the sterile field, and can be placed on a flat, non-sterile surface or may be suspended from a nearby IV pole. The Vasoview Hemopro 3 Power Supply does not make contact with the patient, nor does it deliver energy directly to the patient; energy to the patient is delivered by the Hemopro 3 Harvesting Tool. The Hemopro 3 Power Supply is intended to be used by healthcare professionals in an operating room environment. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00607567701281), received between Jun 29, 2026 and Aug 28, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
1 other recall cover devices cleared under the same FDA submission (K251238); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Failure to Deliver Energy1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 28, 2026Failure to Deliver Energy
MalfunctionJun 29, 2026Break
THE HOSPITAL REPORTED THAT HEMOPRO 3 POWER SUPPLY DID NOT POWER ON. UPON INITIAL INSPECTION, THEY WERE USING A NON-GETINGE POWER CABLE. THEY CANNOT LOCATE THE POWER CABLE THE DEVICE WAS SHIPPED WITH. THEY LOCATED ANOTHER HP3 WITH THE CONNECTED GETINGE POWER CABLE AND CONNECTED IT TO THE POWER SUPPLY. THE DEVICE DID NOT POWER ON. THERE WERE NO SOUNDS COMING FROM THE POWER SUPPLY OR LIGHTS ON. UPON INSPECTION, THE HANDLE/HANGER AT THE TOP OF THE DEVICE IS NOTED TO HAVE A FULL THICKNESS CRACK/BREAK. THESE STEPS AND INSPECTIONS WERE COMPLETED BY THE PRODUCT MANAGER. THEY WERE ASKED IF THE POWER SUPPLY HAD BEEN DROPPED, AND NO ONE COULD CONFIRM. THERE WAS NO ABNORMAL SOUNDS COMING FROM THE POWER SUPPLY. THIS DID NOT INVOLVE A PATIENT OR A SURGICAL CASE. THERE IS NO PATIENT OR CASE DATA TO REPORT. PER THE PHOTO, IT SHOWS THAT THE HANGER AT THE TOP IS CRACKED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25650208 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K251238. One submission often covers many models, so check the product and lot details in each record.
- Z-2636-2025 · Aug 6, 2025 · Open, ClassifiedVasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-6000, VH-6001, and VH-6010) is a
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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