Triple Lumen Sump Drain 0080400Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741050077), received between Jul 10, 2019 and Jul 10, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 18, 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.

• MalfunctionJul 10, 2019Migration or Expulsion of Device; Migration or Expulsion of Device; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE DRAIN SLID OUT THROUGH THE FLANGE.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 8776090 ↗
• MalfunctionJul 10, 2019Restricted Flow rate; Restricted Flow rate; Obstruction of Flow

  IT WAS REPORTED THAT THE DEVICE BECAME BLOCKED/CLOGGED.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 8776087 ↗