Medline MDT24SUPRAAPLRecalls & reported problems
Medline Industries, Inc. · MATTRESS,SYSTEM,SUPRA APL,LAL/ALT. PRESS · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 42
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 42 adverse event reports that list this exact device (DI 10080196372164), received between Mar 4, 2022 and Sep 30, 2026 — classified as 1 injury, 41 malfunctions.
The most frequently reported specific device problem is “Inflation Problem” (18 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Inflation Problem18
- Gas/Air Leak13
- Unintended Deflation4
- Deflation Problem3
- Pumping Problem3
- Decrease in Pressure2
- Electrical /Electronic Property Problem2
- Material Split, Cut or Torn2
Patient problems
- No Clinical Signs, Symptoms or Conditions40
- Discomfort1
- Pressure Sore/Ulcer1
Recent adverse event reports
The 25 most recent of 42 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951022 ↗MalfunctionSep 28, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917970 ↗MalfunctionSep 28, 2026Failure to Pump
It was reported that "Air Mattress motor is making a rattling noise and will not blow air to the mattress and the low pressure light is on."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915881 ↗MalfunctionSep 28, 2026Inflation Problem; Gas/Air Leak
It was reported that "MATTRESS DOES NOT HOLD AIR." It was also reported that "the top mattress baldders is not inflating."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50913248 ↗MalfunctionSep 23, 2026Inflation Problem
It was reported that "The motor is not pushing enough air any longer to keep it inflated firmly."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869992 ↗MalfunctionSep 18, 2026Inflation Problem
It was reported that the mattress is not inflating at all.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50818326 ↗MalfunctionSep 16, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50796833 ↗MalfunctionSep 15, 2026Material Puncture/Hole; Gas/Air Leak; Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50777948 ↗MalfunctionSep 14, 2026Pumping Problem; Noise, Audible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765210 ↗MalfunctionSep 12, 2026Decrease in Pressure; Unintended Deflation
Patient problems: Discomfort
MAUDE report 50746821 ↗MalfunctionSep 9, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50699962 ↗MalfunctionSep 9, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698958 ↗MalfunctionSep 9, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50692872 ↗MalfunctionSep 9, 2026Inflation Problem
It was reported that "MIDDLE CELLS ON THE MATRESS ARE NOT INFLATING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50692344 ↗MalfunctionSep 9, 2026Inflation Problem
It was reported that the pump for this low air loss mattress is not blowing air.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50683007 ↗MalfunctionSep 8, 2026Unexpected Shutdown; Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677931 ↗MalfunctionSep 8, 2026Pumping Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676576 ↗MalfunctionSep 8, 2026Deflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674107 ↗MalfunctionSep 8, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50672870 ↗MalfunctionSep 8, 2026Inflation Problem
It was reported that "MATTRESS NOT INFLAING CORRECTLY. THE MATTRESS INFLATES EVERY OTHER DIVOT".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50671292 ↗MalfunctionSep 8, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50669445 ↗MalfunctionSep 2, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50573171 ↗MalfunctionSep 2, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50572574 ↗MalfunctionSep 2, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50572443 ↗MalfunctionSep 2, 2026Loose or Intermittent Connection; Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50571411 ↗
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 MDT24SUPRADPSMedline Industries, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE40 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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