iGo2 125KRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885304022244), received between Jun 2, 2026 and Jun 2, 2026 — classified as 1 malfunction.

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

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.

• MalfunctionJun 2, 2026Fire; Charging Problem

  DRIVE MEDICAL WAS NOTIFIED OF AN INCIDENT INVOLVING AN OXYGEN CONCENTRATOR BY A PROVIDER, WHO REPORTED THE DEVICE CAUGHT FIRE WHILE THE BATTERY WAS BEING CHARGED. THE END USER WAS NOT CONNECTED TO THE OXYGEN CONCENTRATOR DURING THE INCIDENT. THE END USER WAS NOT INJURED AND DID NOT SEEK MEDICAL ATTENTION. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE MEDICAL WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25364376 ↗