McKesson 22-ES39TRecalls & reported problems
Mckesson Medical-Surgical Inc. · Resistick II Coated Extended Mod Blade Electrode · Class 2
Data updated Oct 16, 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 20612479210107), received between Dec 23, 2020 and Jul 15, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Melted” (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
- Melted1
- Thermal Decomposition of Device1
Patient problems
- Burn, Thermal1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 15, 2025Melted; Melted
COMPLAINANT ALLEGES "ONE OF OUR SURGEONS IS WANTING TO TRY NEW ELECTRODE BLADES SO I ORDERED ARGENT (MCKESSON-HAS BOTH NAMES ON IT) REF # 22-ES39T LOT 1124Z AND WE HAD A MAJOR ISSUE WITH IT DURING A CASE. THE PLASTIC PROTECTOR OVER THE BLADE STARTED TO MELT SO WE DISCONTINUED USING THE PRODUCT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22513201 ↗MalfunctionDec 23, 2020Thermal Decomposition of Device
DURING A PROCEDURE THAT METAL PART OF THE DEVICE BURNED THROUGH THE INSULATION AND CAUSED A SMALL BURN ON THE PATIENT'S SKIN. THE PATIENT DID NOT REQUIRE AN MEDICAL INTERVENTION AND WILL NOT HAVE ANY PERMANENT AFFECT ON THE PATIENT.
Patient problems: Burn, Thermal
MAUDE report 11069454 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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