microAIR MA800Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841447111252), received between Aug 19, 2026 and Aug 19, 2026 — classified as 1 injury.

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.

Most reported problems

Recent adverse event reports

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

• InjuryAug 19, 2026Adverse Event Without Identified Device or Use Problem

  Invacare was made aware on July 23, 2026, of an incident involving a 2-year-old model MA800 Micro Air mattress system. The end-user stated that sometimes the air goes in between the cells and there is a sink in spot in the mattress. After using this mattress for a year, the end user has developed a pressure wound on the left side of his hip. He originally had a lateral rotation mattress because of an open wound on the left hip that did close but has reopened since using the new alternating pressure mattress.

  Patient problems: Pressure Sore/Ulcer

  MAUDE report 50323966 ↗