Owgels Oxygen Concentrator OZ-5-02TW0Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06921141405025), received between Sep 23, 2026 and Sep 23, 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. 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.

• InjurySep 23, 2026Adverse Event Without Identified Device or Use Problem

  (b)(6) reports that he was sitting on his phone playing a game and decided to light a cigarette. He states he forgot he was wearing his NC with oxygen on. When he lit his lighter, the NC produced a fame. He immediately removed the oxygen the oxygen tubing and threw it to the floor then tuned off the oxygen flow. (b)(6) states the flame was extinguished and he had no pain so he did not call VITAS to notify. (b)(6) states he replaced the oxygen tubing. Smoking cessation and xygen safety education was provided by nurse during visit. Per VITAS nurse assessment patient sustained 2nd degree burn to right nare and tip of nostril as evidenced by scab.User Facility/lmporter Report Number: (b)(4).

  Patient problems: Burn(s)

  MAUDE report 50863308 ↗