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CHATTANOOGA 2866Recalls & reported problems

Djo, LLC · SENIOR SOLUTIONS 4CH STIM PKG US STD · Class 2

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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912296793), received between Mar 18, 2022 and Mar 18, 2022 — 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Superficial (First Degree) Burn1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 18, 2022Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE STIM UNIT ALLEGEDLY BURNED THE PATIENT.

    Patient problems: Superficial (First Degree) Burn

    MAUDE report 13805736 ↗

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Sources and updates

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