Medline MDS9543CSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50080196171482), received between Sep 28, 2026 and Sep 28, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 28, 2026Material Separation

  It was reported that "The assembly process has been an inconvenience for the team, but more concerning is that they fall apart during examination. Additionally, the staff has noted significant muffling during auscultation, which makes it difficult to properly assess patients' cardiac status."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50916008 ↗