NAMIC 60160372Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10193489048728), received between Sep 30, 2026 and Sep 30, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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.

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.

• MalfunctionSep 30, 2026Loose or Intermittent Connection

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50952760 ↗
• MalfunctionSep 30, 2026Loss of or Failure to Bond; Fluid/Blood Leak

  It was reported that "It is the 3 way stopcock from the saline to the waste bag. LL does not tighten and is leaking."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50945920 ↗