MEDLINE MDTSUPAIRPRORecalls & reported problems
Medline Industries, Inc. · MATTRESS,SYSTEM,SUPRA AIR PRO,LAL · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10197344102273), received between May 7, 2026 and Sep 16, 2026 — classified as 10 malfunctions.
The most frequently reported specific device problem is “Inflation Problem” (3 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 Problem3
- Decrease in Pressure2
- Gas/Air Leak2
- Defective Alarm1
- Deflation Problem1
- Material Split, Cut or Torn1
- Pumping Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions10
- Discomfort1
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Defective Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794337 ↗MalfunctionSep 9, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698128 ↗MalfunctionSep 9, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50696392 ↗OtherSep 8, 2026Deflation Problem
It was reported that THE MATTRESS NO LONGER HOLDS AIR, IT GOES COMPLETELY FLAT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50670364 ↗MalfunctionSep 8, 2026Decrease in Pressure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50658902 ↗MalfunctionSep 4, 2026Material Split, Cut or Torn
It was reported that "After observing, the clear tape that holds the cells together rips/becomes loose that holds the cells together. Many of the air cells pop out/up high while others are very low and almost look deflated with no air flow".
Patient problems: Discomfort
MAUDE report 50610742 ↗MalfunctionSep 1, 2026Decrease in Pressure
It was reported that the unit no longer holding air. when he puts his hand on the unit it sinks in.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50545053 ↗MalfunctionSep 1, 2026Inflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50543578 ↗MalfunctionAug 31, 2026Inflation Problem
It was reported that 2 cells that have stopped inflating.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50524006 ↗MalfunctionAug 31, 2026Pumping Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50523128 ↗MalfunctionMay 7, 2026Gas/Air Leak
IT WAS REPORTED THAT IT DOES NOT FEEL COMPLETELY FILLED WITH AIR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25117242 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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