Medline MDT24MEDAIRMXRecalls & reported problems
Medline Industries, Inc. · MATTRESS,SYSTEM,MEDTECH MAX,TRUE,36X80 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10080196372058), received between May 17, 2026 and Sep 30, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Material Protrusion/Extrusion” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Material Protrusion/Extrusion2
- Unintended Deflation2
- Decrease in Pressure1
- Gas/Air Leak1
- Inflation Problem1
- Material Puncture/Hole1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Ambulation or Postural Difficulties1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Protrusion/Extrusion
It was reported that MATTRESS HAS A BUBBLE IN THE MIDDLE/OFF TO THE SIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947926 ↗MalfunctionSep 30, 2026Inflation Problem
It was reported that the Item stopped working.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947444 ↗MalfunctionSep 21, 2026Material Protrusion/Extrusion
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50847534 ↗MalfunctionSep 8, 2026Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674279 ↗MalfunctionSep 2, 2026Unintended Deflation
Patient problems: Ambulation or Postural Difficulties
MAUDE report 50569068 ↗MalfunctionMay 17, 2026Decrease in Pressure; Material Puncture/Hole; Gas/Air Leak
IT WAS REPORTED THAT, WHEN PLUGGED IN, THERE IS AN ERROR THAT THERE WAS A LEAK AND FOUND THESE PUNCTURES. ERROR DISPLAYED ON UNIT, NO HOLES FOUND ON MATTRESS. THIS DOESN'T ALLOW MATTRESS TO FUNCTION PROPERLY. THE PATIENT UNABLE TO LAY IN BED DUE TO MATTRESS BEING DEFLATED. THIS CAN LEAD TO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25196508 ↗
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
- Medline MDT24SUPRADPSMedline Industries, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE40 reports
- Synergy® Surface P6881Hill-Rom, Inc. · MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE28 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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