CHATTANOOGA 2302Recalls & reported problems
Djo, LLC · HYDROCOLLATOR, SS-2, C/W 8 STD. PACKS · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912021166), received between Jul 18, 2019 and Jul 18, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Sparking” (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
Device problems
- Sparking1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 18, 2019Sparking; Sparking
IT WAS REPORTED THAT SPARKS WERE COMING OUT FROM THE BOTTOM PART OF THE UNIT. THERE ARE NO REPORTED INJURIES, THE UNIT LOOKS INTACT WITH NO DAMAGED AREAS, AND IT IS NOT LEAKING.
Patient problems: No Patient Involvement
MAUDE report 8802221 ↗
Other UNIT, HEATING, POWERED devices
- CHATTANOOGA 2502Djo, LLC · UNIT, HEATING, POWERED2 reports
- CHATTANOOGA 2402Djo, LLC · UNIT, HEATING, POWERED2 reports
- CHATTANOOGA 2802Djo, LLC · UNIT, HEATING, POWERED1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.