Medline MDS89697Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 40080196746027), received between Aug 24, 2026 and Sep 28, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Activation Problem” (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 28, 2026Sharp Edges

  It was reported that "the edges of her handrails being sharp, ¿knife railings¿.".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50917037 ↗
• MalfunctionSep 22, 2026Unstable

  It was reported that the clamp will not tighten.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50857763 ↗
• MalfunctionAug 27, 2026Unstable

  It was reported that side rails wiggle alot.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50476923 ↗
• MalfunctionAug 27, 2026Activation Problem; Separation Problem

  It was reported that "PER PT SHE HAS HOSPITAL BED W/RAILS ON BOTH SIDES. ONE RAIL FELL OFF AND OTHER IS NOT WORKING."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50476520 ↗
• MalfunctionAug 24, 2026Activation Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50415435 ↗