Devilbiss iGO 306DSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885304002277), received between Sep 1, 2022 and Sep 1, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Melted” (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.

• MalfunctionSep 1, 2022Melted; Melted

  DEVILBISS HEALTHCARE WAS NOTIFIED BY A HOME OXYGEN PROVIDER OF A COMPLAINT INVOLVING A PORTABLE OXYGEN CONCENTRATOR. THE PROVIDER STATED, "WHILE IN USE, THE CHARGER THAT PLUGS INTO DC OUTLET MELTED, CAUSING THE UNIT TO BREAK." THERE WAS NO REPORT OR EVIDENCE OF ILLNESS, INJURY OR MEDICAL TREATMENT ASSOCIATED WITH THE COMPLAINT. THE PORTABLE CONCENTRATOR AND POWER SUPPLY ARE BEING RETURNED TO DEVILBISS FOR EVALUATION. AN UPDATE WILL BE FILED IF NEW INFORMATION BECOMES AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15337172 ↗