DeVilbiss 125D-XBRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885304032045), received between Jul 30, 2026 and Jul 30, 2026 — classified as 1 malfunction.

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

1 other recall cover devices cleared under the same FDA submission (K172648); 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. 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.

• MalfunctionJul 30, 2026Smoking

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50084556 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K172648. One submission often covers many models, so check the product and lot details in each record.

• Z-0229-2023 · Sep 19, 2022 · Open, Classified
  125 series iGO2 Portable Oxygen Concentrator-indicated for the administration of supplemental oxygen. Models: 125D, 125D-XB