Medline RTACIBOMRecalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10193489014310), received between Aug 16, 2026 and Sep 30, 2026 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2026Detachment of Device or Device Component

  It was reported that "The needle on the gauge has come off."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50952430 ↗
• MalfunctionSep 25, 2026Mechanical Jam; Suction Failure

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50902780 ↗
• MalfunctionSep 10, 2026Break; Gas/Air Leak

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50721457 ↗
• MalfunctionSep 9, 2026Suction Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50695421 ↗
• MalfunctionAug 27, 2026Physical Resistance/Sticking

  It was reported that "the unit is not functioning and the knob does not work."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50483998 ↗
• MalfunctionAug 18, 2026Mechanical Jam

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50302528 ↗
• MalfunctionAug 16, 2026Detachment of Device or Device Component

  It was reported that "The needle on the gauge has come off."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50267795 ↗