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AtmosAir 9000 ARecalls & reported problems

Arjohuntleigh AB · AtmosAir 9000 A - Mattress. Available in range of sizes Length 75" - 84" and Width 32" - 38". Options on covers · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055982784986), received between Feb 21, 2020 and Feb 21, 2020 — classified as 1 malfunction.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Fall1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 21, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A PATIENT FELL TWICE FROM THE MATTRESS. THE CARER STATED THERE WAS A "LUMP" IN THE MATTRESS. NO HEALTH CONSEQUENCES WERE REPORTED.

    Patient problems: Fall; No Consequences Or Impact To Patient

    MAUDE report 9738486 ↗

Other MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE devices

All MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE devices →

Sources and updates

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