MEDLINE MDTSUPAIRB42Recalls & reported problems
Medline Industries, Inc. · MATTRESS,BARI SUPRA AIR 42,ALT PRESS · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10197344102136), received between Aug 31, 2026 and Sep 22, 2026 — classified as 10 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (5 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
- Material Split, Cut or Torn5
- Unintended Deflation3
- Gas/Air Leak1
- Inflation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
- Discomfort3
- Hemorrhage/Blood Loss/Bleeding3
- Impaired Healing1
- Tissue Breakdown1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50860378 ↗MalfunctionSep 18, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50826273 ↗MalfunctionSep 15, 2026Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781164 ↗MalfunctionSep 15, 2026Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781163 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: Discomfort; Hemorrhage/Blood Loss/Bleeding
MAUDE report 50700705 ↗MalfunctionSep 8, 2026Material Split, Cut or Torn
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 50671039 ↗MalfunctionSep 1, 2026Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50548504 ↗MalfunctionSep 1, 2026Material Split, Cut or Torn
Patient problems: Discomfort; Impaired Healing
MAUDE report 50543693 ↗MalfunctionSep 1, 2026Material Split, Cut or Torn
Patient problems: Discomfort; Hemorrhage/Blood Loss/Bleeding; Tissue Breakdown
MAUDE report 50542606 ↗MalfunctionAug 31, 2026Inflation Problem
It was reported that "It does not hold air like it should."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50519094 ↗
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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