Medline MDT24SUPRADPSRecalls & reported problems
Medline Industries, Inc. · MATTRESS,SYSTEM,SUPRA DPS,LAL/ALT. PRESS · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 40
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 40 adverse event reports that list this exact device (DI 40080196372196), received between Jun 10, 2020 and Sep 30, 2026 — classified as 39 malfunctions.
The most frequently reported specific device problem is “Inflation Problem” (13 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.
Reports received per month
Most reported problems
Device problems
- Inflation Problem13
- Gas/Air Leak7
- Electrical /Electronic Property Problem5
- Material Puncture/Hole4
- Decrease in Pressure3
- Material Split, Cut or Torn3
- Pumping Problem3
- Deflation Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions37
- Discomfort1
- Fall1
- Laceration(s)1
- Tissue Breakdown1
Recent adverse event reports
The 25 most recent of 40 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Device Alarm System
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951469 ↗MalfunctionSep 30, 2026Decrease in Pressure
It was reported that "Low pressure".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947996 ↗MalfunctionSep 30, 2026Inflation Problem
It was reported that ¿HER MATTRESS THE FIRST 4 DAYS IT WAS WORKING PROPERLY, AFTER THE FIFTH NIGHT MATTRESS WAS INFLATED BUT NOT IN FULL¿ and ¿SHE CHECKED ALL CONNECTIONS AND ALL IS CONNECTED PROPERLY BUT NOT INFLATION IN FULL.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947088 ↗MalfunctionSep 30, 2026Inflation Problem
It was reported that "now the mattress is not holding air at all either".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944916 ↗MalfunctionSep 29, 2026Material Puncture/Hole
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937428 ↗MalfunctionSep 29, 2026Device Alarm System
It was reported that "the pump is beeping saying low air pressure. They hooked another pump up to this bed and it wasn¿t beeping so it appears to be the pump."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932254 ↗MalfunctionSep 29, 2026Gas/Air Leak
It was reported that one or several of the cells are not working.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932082 ↗MalfunctionSep 29, 2026Inflation Problem
This VMSR report summarizes 2 malfunction events that occurred during Q1 2025 ((b)(6) , 2025). The account reported that a mattress system exhibited incomplete inflation, with individual air cells not inflating fully during operation. The customer requested servicing, repair, or replacement of the affected device due to the reported loss of support performance. A mattress information form was requested to obtain additional details regarding the affected unit; however, the completed form was not received. The complaint was subsequently assigned for lot and serial number review. No patient age, weight, sex, race, or ethnicity information was available. No patient or user injuries were reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931887 ↗MalfunctionSep 28, 2026Material Split, Cut or Torn
Patient problems: Discomfort
MAUDE report 50923797 ↗MalfunctionSep 25, 2026Electrical /Electronic Property Problem; Decrease in Pressure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50902448 ↗MalfunctionSep 25, 2026Unintended Deflation
It was reported that the mattress also was not keeping air pressure as well.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50892810 ↗MalfunctionSep 24, 2026Material Puncture/Hole
It was reported that there was a "deflating mattress" and "the pumping tube has a line of tiny punctures that could not be sourced."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50889523 ↗MalfunctionSep 22, 2026Electrical /Electronic Property Problem
It was reported that "The pump is malfunctioning and consistently alarms. There seems to be no loss of air in the mattress."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856587 ↗MalfunctionSep 21, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50848204 ↗MalfunctionSep 21, 2026Material Puncture/Hole
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50847854 ↗MalfunctionSep 21, 2026Noise, Audible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50845705 ↗MalfunctionSep 21, 2026Inflation Problem; Pumping Problem
It was reported that the low air loss mattress was "triggering the service light." The customer also stated, "I've tried it on multiple mattresses and it's doing the same thing."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50844109 ↗MalfunctionSep 21, 2026Inflation Problem
It was reported that "it will not inflate properly" and "it just does not inflate correctly." "I set it up and let it inflate for 45 minutes then I laid on it and I went al the way to the floor."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50840188 ↗MalfunctionSep 17, 2026Electrical /Electronic Property Problem
It was reported that "PUMP NOT WORKING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50802105 ↗MalfunctionSep 14, 2026Pumping Problem; Activation Failure
It was reported that "the lock button should activate after 3 minutes, it does not," "It alarms about a half hour/hour later," and "I have tried on different mattresses, but 3 pumps keep doing the same thing."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756379 ↗MalfunctionSep 14, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756010 ↗MalfunctionSep 13, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50747765 ↗MalfunctionSep 10, 2026Deflation Problem; Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50718120 ↗MalfunctionSep 10, 2026Material Puncture/Hole
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50716987 ↗MalfunctionSep 8, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677501 ↗
Other MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE devices
- Medline MDT24A20Medline Industries, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE267 reports
- Medline MDT24A10Medline Industries, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE118 reports
- Guardian GS-2.5-CTurncare Inc · Mattress, Air Flotation, Alternating Pressure2 recalls15 reports
- IsoAir 2941Stryker Corporation · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE1 recall1 report
- Arise 1000 EX AREXLAL-CUJoerns Healthcare, LLC · Mattress, Air Flotation, Alternating Pressure1 recall0 reports
- Medline MDT24SUPRAAPLMedline Industries, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE42 reports
- Synergy® Surface P6881Hill-Rom, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE28 reports
- NIMBUS 650001DARArjohuntleigh AB · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE2 deaths17 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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