Honeywell HWM705BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00092926007058), received between Jun 9, 2022 and Jun 9, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Device Handling 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. 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.

• InjuryJun 9, 2022Use of Device Problem; Device Handling Problem; Patient Device Interaction Problem; Use of Device Problem; Device Handling Problem; Patient Device Interaction Problem

  A CONSUMER REPORTED THAT HER DAUGHTER RECEIVED SEVERE BURNS ON HER ARM, HAND, AND WRIST ARE FROM HOT STEAM COMING FROM A WARM MIST HUMIDIFIER DURING USE. MEDICAL INTERVENTION WAS SOUGHT FOR HER INJURIES, AS WELL AS FOLLOW-UP CARE VISITS WITH BURN SPECIALISTS. THE PRODUCT DISPLAYS A CLEAR WARNING ON THE CORD THAT STATES, "WARNING KEEP OUT OF REACH OF CHILDREN HOT STEAM CAN CAUSE SERIOUS BURN INJURY" AND THE INSTRUCTIONS FOR PROPER USE ALSO HAVE CLEAR WARNINGS THAT STATE "WARNING: KEEP OUT OF REACH OF CHILDREN AND PETS. THIS PRODUCT PRODUCES HOT STEAM AND SHOULD BE PLACED IN AN AREA NOT ACCESSIBLE TO CHILDREN OR PETS. ENSURE THE POWER CORD IS ALSO SECURELY OUT OF REACH". KAZ USA, INC. HAS REQUESTED THAT THE PRODUCT BE RETURNED TO OUR COMPANY FOR TESTING.

  Patient problems: Burn(s); Full thickness (Third Degree) Burn; Partial thickness (Second Degree) Burn

  MAUDE report 14647173 ↗