Inogen One G3 Oxygen Concentrator 1050 (REF IO-300)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00817131020056), received between Mar 7, 2022 and Mar 7, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fire” (1 report).

1 other recall cover devices cleared under the same FDA submission (K032818); they may or may not involve this specific model.

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 18, 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.

• InjuryMar 7, 2022Fire; Fire

  IT WAS REPORTED THE PATIENT EXPERIENCED A HOUSE FIRE. REPORTEDLY, THE PATIENT PLUGGED THE PORTABLE OXYGEN CONCENTRATOR INTO A POWER STRIP. AS A RESULT, THE PATIENT WAS SENT TO THE HOSPITAL FOR SMOKE IN HER LUNGS. IN TURN, THE PATIENT WAS STABLE AT HOME.

  Patient problems: Low Oxygen Saturation

  MAUDE report 13685059 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K032818. One submission often covers many models, so check the product and lot details in each record.

• Z-1368-05 · Aug 1, 2005 · Terminated
  Portable Oxygen Generator