Medline MDT24A20PUMPRecalls & reported problems
Medline Industries, Inc. · PUMP,REPLACEMENT,A20,LAL/ALTERNATING · Class 2
Data updated Oct 13, 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 10884389945896), received between Sep 1, 2026 and Sep 24, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Unintended Deflation” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Deflation3
- Deflation Problem1
- Failure to Power Up1
- Inflation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Failure to Power Up
It was reported that: "New pump failure out of the box today. Pump does not work."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885366 ↗MalfunctionSep 17, 2026Unintended Deflation
It was reported that "The mattressws are not staying inflated properly. They are going flat" and "When they are changing / rotating they don¿t fill correctly."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50803421 ↗MalfunctionSep 9, 2026Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50698540 ↗MalfunctionSep 1, 2026Unintended Deflation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50550535 ↗MalfunctionSep 1, 2026Inflation Problem
It was reported that ¿THE PUMP DOES NOT FULLY INFLATE THE MATTRESS HOWEVER DOES CONTINUED TO RUN.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50545933 ↗MalfunctionSep 1, 2026Deflation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50542903 ↗
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 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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