NAMIC 80058307Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 20193489066705), received between Sep 22, 2026 and Sep 29, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Detachment of Device or Device Component

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50937032 ↗
• MalfunctionSep 23, 2026Detachment of Device or Device Component

  It was reported that "During the procedure, the ring detaches from the crane block".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50872502 ↗
• MalfunctionSep 22, 2026Detachment of Device or Device Component

  It was reported that "During the procedure, the ring detaches from the tap block (see photo)."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50854266 ↗