V. Mueller LA8506Recalls & reported problems
Steris Corporation · V. Mueller ANGLED inchesV inches HOOK ELECTRODE 33CM · 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 10885403053917), received between May 12, 2021 and May 12, 2021 — 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 12, 2021Sparking; Sparking
INSTRUMENT APPEARS TO BE FRAYING AND STARTED SPARKING DURING THE PROCEDURE. THEY ARE NOT SURE IF THIS ITEM IS FLAWED, OR IF THEY ARE USING IT WRONG. IT APPEARS THE INSULATION ON THE LOWER PORTION OF THE INSTRUMENT HAS COME OFF WHICH ALLOWS THE INSTRUMENT TO SPARK WHEN BEING USED ON LAPAROSCOPIC CASES. THERE WAS NOT ANY DAMAGE OR PATIENT OR USER INJURY. NO FURTHER INFORMATION AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11815739 ↗
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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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