CHATTANOOGA 2402Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888912021449), received between Nov 5, 2019 and Dec 2, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Smoking” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 2, 2025Smoking; Temperature Problem; Smoking; Temperature Problem

  IT WAS REPORTED THAT THE UNIT OVERHEATING ON LOW THERMOSTAT SETTING, REPORTED THAT ON MONDAY (B)(6) 2025 THE FOOTBALL COACH STATED THAT HE WALKED INTO THE TRAINING ROOM AND SAW BLACK SMOKE COMING FROM THE HYDROCOLLATOR. HE OPENED IT UP AND SMOKE CAME ROLLING OUT. IT WAS UNPLUGGED AND IT WAS TAKEN OUTSIDE, FIRE DEPARTMENT WAS CONTACTED AND THEY DID NOT HAVE A REPORT, NO INJURY OR DAMAGES OCCURRED AT THE TIME OF THE INCIDENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23700710 ↗
• InjuryNov 5, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PHYSIOTHERAPIST EXPERIENCED UNSPECIFIED BURNS DURING A TREATMENT. THE COMPLAINT REPORT SUGGESTS, BUT DOES NOT EXPLICITLY STATE, THAT MEDICAL INTERVENTION WAS REQUIRED TO PREVENT PERMANENT IMPAIRMENT. NO FURTHER INFORMATION IS CURRENTLY AVAILABLE.

  Patient problems: Burn(s)

  MAUDE report 9280514 ↗