CHATTANOOGA 7560Recalls & reported problems
Djo, LLC · INTELECT 4CH STIM PKG · 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 00888912372817), received between May 9, 2016 and May 9, 2016 — 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
- Lead(s), Burn(s) From1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 9, 2016Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
COMPLAINT RECEIVED THAT ALLEGES "ELECTRODES WERE GETTING UNCOMFORTABLY HOT. THE CUSTOMER TURNED THE UNIT DOWN TO LEVEL ONE, THEN TURNED THE UNIT OFF. THE ELECTRODES SHOCKED THE CUSTOMER AS HE REMOVED THE ELECTRODES FROM THE PATIENT. THE LOWER TWO ELECTRODES WERE VERY HOT. AT THE NEXT VISIT THE PATIENT MADE CUSTOMER AWARE OF BLISTERS AT THE SITE OF THE INJURY. THE PATIENT CAME IN ON FRIDAY (B)(6) 2016 WITH OPEN WOUNDS. CUSTOMER IS CALLING A WOUND CENTER". QUESTIONNAIRE NOT RECEIVED FROM CLINICIAN AND/OR PATIENT. DEVICE NOT RETURNED TO MANUFACTURER FOR EVALUATION.
Patient problems: Lead(s), Burn(s) From
MAUDE report 5640861 ↗
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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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