Medline RTACIDCMRecalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10193489014334), received between Sep 2, 2026 and Sep 30, 2026 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Break” (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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50952489 ↗
• MalfunctionSep 22, 2026Crack

  It was reported that BACK MOUNTING PLATE LOWER BOTTOM POTION SPIKET. BOTTOM PLASTIC SPREADER PIECE NOT WORKING/DAMED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50856495 ↗
• MalfunctionSep 18, 2026Break; Contamination

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50820645 ↗
• MalfunctionSep 11, 2026Suction Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50734663 ↗
• MalfunctionSep 9, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50696580 ↗
• MalfunctionSep 2, 2026Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50570433 ↗