ReNew 6924Recalls & reported problems
Microline Surgical, Inc. · Electrocautery Probe, 34cm, Reusable · Class 2
All models of ReNew (45)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00811099010913), received between Nov 2, 2018 and May 20, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Arcing” (1 report).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Arcing1
- Insufficient Device Problem Information1
- Unintended Electrical Shock1
Patient problems
- Burn(s)1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 20, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
BURNED A PATIENT, RE-INSTALLED L-HOOK AND TIP WAS FINE.
Patient problems: Burn(s)
MAUDE report 19353368 ↗MalfunctionAug 10, 2021Arcing; Arcing
THE CAUTERY PROBE AND L HOOK WERE BEING USED ON 90 AND SPRAY TO COAGULATE A LIVER BLEED WHEN THE INSTRUMENT MELTED AND ARCHED FROM THE SIDE BURNING AN UNINTENDED PORTION OF THE LIVER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12300014 ↗MalfunctionNov 2, 2018Unintended Electrical Shock; Unintended Electrical Shock
DURING A SURGICAL PROCEDURE, THE CLINICIAN EXPERIENCED AN ELECTRICAL PULSE FEEDBACK THROUGH THE RENEW ELECTROCAUTERY PROBE. THERE WAS NO HARM TO THE PATIENT OR USER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8033123 ↗
Other Electrosurgical, Cutting & Coagulation & Accessories devices
- Vasoview Hemopro 2 VH-4000Maquet Cardiovascular LLC · Electrosurgical, Cutting & Coagulation & Accessories6 recalls1 death3,232 reports
- LigaSure LF1937Covidien LP · Electrosurgical, cutting & coagulation & accessories3 deaths2,090 reports
- Olympus WB91051WOLYMPUS Winter & Ibe GmbH · Electrosurgical, Cutting & Coagulation & Accessories1 death1,951 reports
- Valleylab FT10 VLFT10GENCovidien LP · Electrosurgical, cutting & coagulation & accessories1 recall5 deaths1,062 reports
- LigaSure LF1837Covidien LP · ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 recall967 reports
- LigaSure LF2019Covidien LP · Electrosurgical, cutting & coagulation & accessories948 reports
- VAPR 225028Depuy Mitek, LLC · ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES895 reports
- LigaSure LF1923Covidien LP · Electrosurgical, cutting & coagulation & accessories855 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page