ATTUNE 2504-40-404Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295438021), received between Aug 20, 2019 and Sep 29, 2022 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Corroded” (4 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 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2022Corroded; Corroded

  IT WAS REPORTED THAT THE DEVICE HAS RUSTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15503883 ↗
• MalfunctionJul 13, 2022Corroded; Corroded

  IT WAS REPORTED THAT THE INSTRUMENTS ARE SHOWING RUST.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15001401 ↗
• MalfunctionAug 20, 2019Corroded; Corroded

  THERE IS RUST ON THE BLACK CLIP.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8912760 ↗
• MalfunctionAug 20, 2019Corroded; Corroded

  THERE IS RUST ON THE LASER MARKING. ALSO THERE IS RUST DEBRIS ON THE BLACK HANDLE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8912645 ↗