Medline RTACIAAARecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10193489014228), received between Aug 25, 2026 and Sep 18, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Break” (2 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 18, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50828692 ↗
• MalfunctionSep 9, 2026Physical Resistance/Sticking

  It was reported that "the knob on the front will not adjust the pressure.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50692114 ↗
• MalfunctionSep 1, 2026Detachment of Device or Device Component; Material Deformation

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50548490 ↗
• MalfunctionAug 26, 2026Incorrect, Inadequate or Imprecise Result or Readings

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50457965 ↗
• MalfunctionAug 25, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50440161 ↗