HemoPro Power Supply C-VH-3010Recalls & reported problems

Summary

The FDA's MAUDE database contains 405 adverse event reports that list this exact device (DI 00607567700826), received between Jul 30, 2020 and Sep 25, 2026 — classified as 7 injuries, 398 malfunctions.

The most frequently reported specific device problem is “Failure to Deliver Energy” (155 reports).

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.

Most reported problems

Recent adverse event reports

The 25 most recent of 405 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 25, 2026Intermittent Loss of Power

  The hospital reported that the T.W. Power Supply had low output. The item was being evaluated by Biomed for repair; however, no specific procedure or case in which the product failed to perform was identified. The product is older and may be due for replacement. No patient or specific case information was provided. No patient effects were reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50895278 ↗
• MalfunctionSep 25, 2026Electrical /Electronic Property Problem

  The hospital reported that the T.W. Power Supply stopped heating/cutting/working. Lights of the power supply were lit but no power at the output. The power supply was the only thing that (when traded out) fixed the problem. Power setting was at 3. The issue occurred during the attempt to cauterize the first branch. The device did not shut off after the 15-second activation cycle and was not able to be reactivated after releasing and reengaging the toggle. The age of the HemoPro Power Supply, Extension Cable, and Adapter is unknown, The power supply was placed on the video tower along with the other video equipment during use. The procedure was finished using a different power supply. A few minutes added to time of case due to troubleshooting cables, and kit vs power supply. No patient harm reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50894736 ↗
• MalfunctionSep 22, 2026Failure to Deliver Energy

  The hospital reported that the T.W. Power Supply began malfunctioning during a CABG procedure. The issue was noticed during sputtering when delivering energy. The customer did not report any information regarding beeping tones. Exchanging the cables/adapters did not resolve the issue; however, using a different power supply did. Power setting at 3. The HemoPro Power Supply was first put into distribution in 2015 The dates for the HemoPro Extension Cable and Adapter are unknown; therefore, their ages cannot be determined. The power supply was placed on the endoscopic tower during use. It was not located in close proximity to other power-generating devices or equipment that would be expected to generate a significant amount of electrical power or cause interference. Minor delay of 2-3 minutes. No patient harm.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50852350 ↗
• MalfunctionSep 2, 2026Electrical /Electronic Property Problem

  The hospital reported that the T.W. Power Supply was not working correctly during the procedure. The problem that occurred was that the device was not cauterizing. Power setting at 3. There was no change in the power settings, and no adjustment to the settings resolved the issue. The power supply was placed on a shelf near the Bovie machine that was not on. The extension cable, adapter, and new harvesting tool kits were changed out; however, the issue persisted and the attempts were unsuccessful. A new device was used to complete the procedure, There was no patient harm. There was a small procedural delay, as the harvest time was lengthened to obtain another device. The power supply is a 2023 unit There is no way of knowing how old their cables and adaptors are because they don't have serial numbers on them.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50559811 ↗
• MalfunctionSep 1, 2026Electrical /Electronic Property Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50542952 ↗
• MalfunctionAug 24, 2026Intermittent Loss of Power

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50403952 ↗
• MalfunctionAug 21, 2026Electrical /Electronic Property Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50366340 ↗
• MalfunctionAug 13, 2026Electrical /Electronic Property Problem

  n/a

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50233517 ↗
• MalfunctionAug 12, 2026Electrical /Electronic Property Problem

  N/A

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50219261 ↗
• MalfunctionJul 31, 2026Intermittent Continuity

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50096041 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED THAT T.W. POWER SUPPLY FAILED WHEN PERFORMING HIGH CURRENT OUTPUT FUNCTIONAL TEST. THE READINGS WERE 5.2-5.3 WHICH IS OUTSIDE OF THE SPECIFICATIONS LISTED IN THE IFU. NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THE FUNCTIONALITY ISSUES WERE OBSERVED BY THE BIOMED. THERE WAS NO PATIENT INVOLVEMENT. THIS POWER SUPPLY WAS PURCHASED ON 7/23/2026. THE TEST WAS PERFORMED PER THE IFU DIRECTIONS. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25210683 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED THAT T.W. POWER SUPPLY FAILED WHEN PERFORMING HIGH CURRENT OUTPUT FUNCTIONAL TEST. THE READINGS WERE 5.2-5.3 WHICH IS OUTSIDE OF THE SPECIFICATIONS LISTED IN THE IFU. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THIS POWER SUPPLY WAS PURCHASED (B)(6) 2026. THE TEST WAS PERFORMED PER THE IFU DIRECTIONS. THE FUNCTIONALITY ISSUES WERE OBSERVED BY THE BIOMED. NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE, THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25210681 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED WHEN PERFORMING HIGH CURRENT OUTPUT FUNCTIONAL TEST ON T.W. POWER SUPPLY AS PER IFU, THE DEVICE FAILED WITH READINGS OF 5.2-5.3 FALLING OUTSIDE OF SPECS LISTED IN IFU. THIS WAS NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE. THIS POWER SUPPLY WAS PURCHASED 3/31/2026. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THE FUNCTIONALITY ISSUES WERE OBSERVED BY BIOMED. THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW OF HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25210680 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED THAT THE T.W. POWER SUPPLY FAILED DURING A HIGH-CURRENT OUTPUT FUNCTIONAL TEST PERFORMED IN ACCORDANCE WITH THE IFU, WITH READINGS OF 5.2¿5.3 FALLING OUTSIDE THE SPECIFICATIONS LISTED IN THE IFU. THIS WAS NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THE FUNCTIONALITY ISSUES WERE OBSERVED BY BIOMED. THIS POWER SUPPLY WAS PURCHASED (B)(6) 2026. THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW OF HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25206137 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED THAT THE T.W. POWER SUPPLY FAILED DURING A HIGH-CURRENT OUTPUT FUNCTIONAL TEST PERFORMED IN ACCORDANCE WITH THE IFU, WITH READINGS OF 5.2¿5.3 FALLING OUTSIDE THE SPECIFICATIONS LISTED IN THE IFU. THIS WAS NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE, IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THIS POWER SUPPLY WAS PURCHASED 3/31/2026. THE FUNCTIONALITY ISSUES WERE OBSERVED BY BIOMED. THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW OF HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25204496 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED WHEN PERFORMING HIGH CURRENT OUTPUT FUNCTIONAL TEST ON T.W. POWER SUPPLY AS PER IFU, THE DEVICE FAILED WITH READINGS OF 5.2-5.3 FALLING OUTSIDE OF SPECS LISTED IN IFU. THE FUNCTIONALITY ISSUES WERE OBSERVED BY BIOMED. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THIS WAS NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE, THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW OF HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25204408 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED DURING A PROCEDURE, THE T.W. POWER SUPPLY ¿KEPT STALLING¿. ANOTHER T.W. POWER SUPPLY WAS USED TO COMPLETE THE PROCEDURE, NO PATIENT EFFECTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25199868 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED WHEN PERFORMING HIGH CURRENT OUTPUT FUNCTIONAL TEST ON POWER SUPPLY AS PER IFU, THE DEVICE FAILED WITH READINGS OF 5.2-5.3 FALLING OUTSIDE OF SPECS LISTED IN IFU. THE FUNCTIONALITY ISSUES WERE OBSERVED BY BIOMED. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THE POWER SUPPLY IS NO LONGER UNDER WARRANTY AS IT WAS PURCHASED (B)(6) 2026. THIS WAS NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE, THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW OF HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25199756 ↗
• MalfunctionMay 18, 2026Intermittent Loss of Power

  THE HOSPITAL REPORTED WHEN PERFORMING HIGH CURRENT OUTPUT FUNCTIONAL TEST ON T.W. POWER SUPPLY AS PER IFU, THE DEVICE FAILED WITH READINGS OF 5.2-5.3 FALLING OUTSIDE OF SPECS LISTED IN IFU. THE FUNCTIONALITY ISSUES WERE OBSERVED BY BIOMED. IT IS UNKNOWN HOW MANY TIMES THE DEVICES WERE IN SERVICE AND USED. THE POWER SUPPLY IS NO LONGER UNDER WARRANTY AS IT WAS PURCHASED (B)(6) 2026. THIS WAS NOTICED DURING BIOMED PERFORMING YEARLY PM ON EQUIPMENT NOT DURING A PROCEDURE, THERE WAS NO PATIENT INVOLVEMENT. THE SAME PERSON TESTED ALL THE POWER SUPPLIES TOGETHER AND HAD ANOTHER TECH REVIEW OF HIS WORK AFTER HIM TO VERIFY RESULTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25199666 ↗
• MalfunctionMay 15, 2026Electrical /Electronic Property Problem

  THE HOSPITAL REPORTED THE T.W. POWER SUPPLY FUNCTIONED FOR A PERIOD OF TIME BEFORE BECOMING INTERMITTENT, AND ULTIMATELY FAILED COMPLETELY DURING A PROCEDURE. IT'S UNKNOWN IF THE PRE-TEST WAS DONE. THE EXTENSION CABLE WAS CHANGED, AND THE ISSUE PERSISTED. IT'S UNKNOWN IF THE DEVICE SHUT OFF AFTER 15 SECONDS. POLYFUSE DOES NOT HAVE A USER INDICATOR. CONTINUED WITH INTERMITTENT POWER. POWER SETTING AT 3. NO CHANGE IN POWER SETTINGS ATTEMPTED. THE AGE OF THE ADAPTOR CABLE AND EXTENSION CABLE IS UNKNOWN. THE POWER SUPPLY IS ON TOWER WITH OTHER EQUIPMENT. NO PROCEDURAL DELAY ASIDE FROM TIME TO TROUBLESHOOT WITH CHANGED CORDS, AND THEN BRINGING IN A DIFFERENT VH-3010. THE VH-3010 FAILED THE SERVICE POWER TESTS PREFORMED BY BIOMED. NO PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25193074 ↗
• MalfunctionMay 15, 2026Failure to Deliver Energy

  THE HOSPITAL REPORTED THAT DURING AN ENDOSCOPIC VEIN HARVESTING PROCEDURE USING THE T.W. POWER SUPPLY, IT'S NO LONGER ABLE TO POWER ON. THE PROBLEM WAS DISCOVERED AFTER SEVERAL INSTANCES OF UNSUCCESSFUL CAUTERIZATION. THEY CONSIDERED AND CHECKED FOR POSSIBLE ISSUES WITH THE ADAPTER CABLE, EXTENSION CABLE, AND CONSUMABLES, BUT IT WAS DETERMINED THAT THE POWER SUPPLY WAS FAULTY. THE OUTPUT SETTING WAS SET TO 3. UNKNOWN IF PRE-CAUTERY TEST WAS PERFORMED. THE PROCESS WAS COMPLETED USING THE SAME EQUIPMENT. THERE ARE NO MAJOR DELAYS. NO HARM WAS DONE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25191638 ↗
• MalfunctionMay 11, 2026Intermittent Continuity

  THE HOSPITAL REPORTED THAT DURING SURGERY, T.W. POWER SUPPLY WAS WORKING INTERMITTENTLY. CABLE AND ADAPTOR WERE SWAPPED DURING TROUBLESHOOTING. NEW DEVICE WAS USED TO FINISH THE PROCEDURE AND IT WORKED FINE. NO PATIENT HARM, NO DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25141361 ↗
• MalfunctionMay 11, 2026Failure to Deliver Energy

  THE HOSPITAL REPORTED THAT T.W. POWER SUPPLY HAD NO POWER. PROBLEM WAS DISCOVERED DURING PREPARATION FOR A PROCEDURE, NO PATIENT EFFECTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25136499 ↗
• MalfunctionMay 11, 2026Intermittent Continuity

  THE HOSPITAL REPORTED THAT AT THE BEGINNING OF THE PROCEDURE THE CAUTERY OF THE VASOVIEW HEMOPRO 2 KEPT CUTTING IN AND OUT DURING POINT OF USE. EXTENSION CORD WAS REPLACED BUT ISSUE KEPT OCCURRING. A NEW T.W. POWER SUPPLY WAS SUBSTITUTED WHICH RESOLVED THE PROBLEM. BEEPING WAS HEARD INTERMITTENTLY. T.W. POWER SUPPLY SET AT LEVEL 2. PRE-CAUTERY TEST NOT PERFORMED. PATIENT WAS NOT INJURED DURING THE CASE. NO PROCEDURAL DELAY WAS INDICATED. THE DEVICE DID NOT SHUT OFF AFTER THE 15-SECOND ACTIVATION CYCLE. POWER SETTING AT 2. THERE WAS NO CHANGE IN SETTINGS THAT RESOLVED THIS ISSUE. THE POWER SUPPLY WAS PLACED ON THE TOWER NEAR THE LIGHT SOURCE AND C02 INSUFFLATOR, AS IN EVERY OTHER HOSPITAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25135359 ↗
• MalfunctionMay 7, 2026Insufficient Device Problem Information

  THE HOSPITAL REPORTED THAT T.W. POWER SUPPLY IS NOT WORKING. THE PROBLEM WAS DISCOVERED WHILE PREPARING FOR A PROCEDURE. THE CUSTOMER IS NOT AWARE OF ANY PATIENT AFFECTS.

  Patient problems: Insufficient Information

  MAUDE report 25113138 ↗