McKesson 22-ES58TRecalls & reported problems
Mckesson Medical-Surgical Inc. · Resistick II Coated Blade Electrode · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20612479210084), received between Feb 15, 2022 and Feb 15, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Loose or Intermittent Connection1
- Physical Resistance/Sticking1
Patient problems
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 15, 2022Loose or Intermittent Connection; Physical Resistance/Sticking
THE CUSTOMER ALLEGED THAT THE PRODUCT IS STICKING WHEN ACTIVATED, WHICH IS CAUSING MORE BLEEDING. ADDITIONALLY, THE PRODUCT GETS PULLED OUT OF THE HANDPIECE AND INTO THE SURGICAL FIELD.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 13537117 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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