CHATTANOOGA 2802Recalls & reported problems
Djo, LLC · HYDROCOLLATOR, E-2, C/W 6 ASSORTED PACKS · Class 1
All models of CHATTANOOGA (39)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00888912022101), received between May 20, 2019 and May 20, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (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
Device problems
- Overheating of Device1
- Temperature Problem1
Patient problems
- No Patient Involvement1
- Patient Problem/Medical Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 20, 2019Overheating of Device; Temperature Problem; Overheating of Device; Temperature Problem
IT WAS REPORTED THAT "THE POWER PLUG CONNECTOR AND POWER CORD PLUG ON THE BACK OF THE UNIT MELTED". THERE WAS NO REPORTED PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement; Patient Problem/Medical Problem
MAUDE report 8625118 ↗
Other UNIT, HEATING, POWERED devices
- CHATTANOOGA 2502Djo, LLC · UNIT, HEATING, POWERED2 reports
- CHATTANOOGA 2402Djo, LLC · UNIT, HEATING, POWERED2 reports
- CHATTANOOGA 2302Djo, LLC · UNIT, HEATING, POWERED1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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