McKesson 22-ESP6HRecalls & reported problems
Mckesson Medical-Surgical Inc. · ELECTROSURGICAL ROCKER PENCIL W/HOLSTER · Class 2
Data updated Oct 16, 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 10612479209180), received between Nov 22, 2023 and Nov 22, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Sparking” (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
- Sparking1
Patient problems
- Superficial (First Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 22, 2023Sparking; Sparking
CUSTOMER "ALLEGED" THAT WHEN USING A 22-ESP6H WITH A REPLACED ELECTRODE DURING A BREAST REDUCTION, THE PATIENT RECEIVED BURNS FROM SPARKS COMING FROM WHERE THE TIP MEETS THE HANDPIECE. THERE WAS NO ADDITIONAL PATIENT HARM.
Patient problems: Superficial (First Degree) Burn
MAUDE report 18193885 ↗
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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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