Valleylab E2999Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884524001838), received between Jul 3, 2018 and Apr 11, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fire” (2 reports).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 11, 2019Fire; Fire

  ACCORDING TO THE REPORTER, INTRA OPERATIVELY, A FLAME WAS PRODUCED AT THE DISTAL END OF THE DEVICE CABLE.

  Patient problems: No Information

  MAUDE report 8503714 ↗
• MalfunctionJul 3, 2018Fire; Fire

  ACCORDING TO THE REPORTER, DURING PROCEDURE, WHEN THE DEVICE WAS ACTIVATED, A SPARK/FIRE WAS SEEN AT THE POINT OF CONNECTION BETWEEN ROBOTIC ARM AND MONOPOLAR CORD. THERE WAS NO PATIENT INJURY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7658115 ↗