Medline MDT24B42Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10080196371945), received between Aug 31, 2026 and Sep 9, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Decrease in Pressure” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 9, 2026Material Puncture/Hole

  It was reported that "The item arrived damaged, there is a hole that is clearly not a natural low air loss hole, it is visibly a damaged area."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50691355 ↗
• MalfunctionSep 2, 2026Inflation Problem; Decrease in Pressure

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50572998 ↗
• MalfunctionAug 31, 2026Gas/Air Leak

  It was reported that AIR IS LEAKING OUT AT THE SEAMS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50531336 ↗
• MalfunctionAug 31, 2026Pressure Problem

  It was reported that "The air mattress from the other unit we have will not hold air when weight is on it. It airs up quick and holds air until we put weight on it then it bottoms out and doesn¿t recover until we take the weight back off."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50524844 ↗