Neptune 2 0702020000Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613154688289), received between Jan 13, 2020 and Jan 13, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Suction Failure” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionJan 13, 2020Suction Failure; Suction Failure

  IT WAS REPORTED THAT DURING A NEUROVASCULAR PROCEDURE PERFORMED BY THE NEUROSURGERY DEPARTMENT AT THE USER FACILITY, THE MANIFOLD CLOGGED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT A CLINICALLY SIGNIFICANT DELAY; NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9580445 ↗
• MalfunctionJan 13, 2020Suction Failure; Suction Failure

  IT WAS REPORTED THAT DURING A NEUROVASCULAR PROCEDURE PERFORMED BY THE NEUROSURGERY DEPARTMENT AT THE USER FACILITY, THE MANIFOLD CLOGGED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT A CLINICALLY SIGNIFICANT DELAY; NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9580443 ↗