CHATTANOOGARecalls & reported problems across all models
Djo, LLC · 39 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 122
- Deaths reported
- 0
- Injuries reported
- 57
- Recalls
- 0
We found 39 models of CHATTANOOGA by Djo, LLC in the FDA's device registry (GUDID). Together they are named in 122 adverse event reports in the FDA's MAUDE database, received between May 9, 2016 and May 31, 2026 — classified as 57 injuries, 65 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (15 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported CHATTANOOGA problems
Device problems
- Adverse Event Without Identified Device or Use Problem44
- Overheating of Device15
- Intermittent Energy Output10
- Patient Device Interaction Problem10
- Electrical /Electronic Property Problem7
- Temperature Problem7
- Smoking6
- Energy Output Problem4
Patient problems
- Burn(s)27
- No Known Impact Or Consequence To Patient19
- No Consequences Or Impact To Patient14
- Electric Shock10
- Partial thickness (Second Degree) Burn10
- No Patient Involvement8
- Superficial (First Degree) Burn8
- Full thickness (Third Degree) Burn6
CHATTANOOGA models
39 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CHATTANOOGA 2738STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT16 reports
- CHATTANOOGA 2760STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT15 reports
- CHATTANOOGA 2783STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT9 reports
- CHATTANOOGA 2761STIMULATOR, NEUROMUSCULAR, EXTERNAL FUNCTIONAL7 reports
- CHATTANOOGA 6000Stimulator, muscle, powered7 reports
- CHATTANOOGA 1032PAD, HEATING, POWERED6 reports
- CHATTANOOGA 27335Ultrasonic diathermy for use in applying therapeutic deep heat6 reports
- CHATTANOOGA 2763STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT6 reports
- CHATTANOOGA 2786Stimulator, muscle, powered6 reports
- CHATTANOOGA 2841EQUIPMENT, TRACTION, POWERED5 reports
- CHATTANOOGA 1033PAD, HEATING, POWERED3 reports
- CHATTANOOGA 27812Lamp, infrared, therapeutic heating3 reports
- CHATTANOOGA 2872STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT3 reports
- CHATTANOOGA FLU115DUnit, fluidotherapy2 reports
- CHATTANOOGA 2402UNIT, HEATING, POWERED2 reports
- CHATTANOOGA 2502UNIT, HEATING, POWERED2 reports
- CHATTANOOGA 27840Lamp, infrared, therapeutic heating2 reports
- CHATTANOOGA FLU110DUnit, fluidotherapy1 report
- CHATTANOOGA 2176KITMassager, therapeutic, electric1 report
- CHATTANOOGA 4738STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2302UNIT, HEATING, POWERED1 report
- CHATTANOOGA 27383Ultrasonic diathermy for use in applying therapeutic deep heat1 report
- CHATTANOOGA 2782Ultrasonic diathermy for use in applying therapeutic deep heat1 report
- CHATTANOOGA 2802UNIT, HEATING, POWERED1 report
- CHATTANOOGA 4759EQUIPMENT, TRACTION, POWERED1 report
- CHATTANOOGA 5000022Device, Iontophoresis, Other Uses1 report
- CHATTANOOGA 1600DIATHERMY, SHORTWAVE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 27816Lamp, infrared, therapeutic heating1 report
- CHATTANOOGA 2788STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2792STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2796STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2798STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2863STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2866STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 39-0700DIATHERMY, SHORTWAVE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 42209ELECTRODE, CUTANEOUS1 report
- CHATTANOOGA 59005ELECTRODE, CUTANEOUS1 report
- CHATTANOOGA 7560STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF1 report
- CHATTANOOGA 8250EQUIPMENT, TRACTION, POWERED1 report
Recent CHATTANOOGA adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMay 31, 2026Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT SUSTAINED A BURN DURING TREATMENT.
Patient problems: Burn(s)
MAUDE report 25342861 ↗InjuryFeb 6, 2026Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT SUSTAINED A BURN DURING TREATMENT.
Patient problems: Burn(s)
MAUDE report 24285047 ↗InjuryDec 8, 2025Temperature Problem; Temperature Problem
CUSTOMER REPORTS INJURY TO CUSTOMER, CUSTOMER REPORTED FRICTION TYPE BURNS ON HER RIGHT-SIDE MID BACK DAYS AFTER TREATMENT WITH RPW2 2176KIT SN (B)(6). CUSTOMER REPORTS NO ANOMALIES WITH UNIT, NO MEDICAL TREATMENT RENDERED.
Patient problems: Burn(s)
MAUDE report 23737952 ↗InjuryDec 8, 2025Temperature Problem; Temperature Problem
IT WAS REPORTED THAT THE PATIENT HAD A SKIN BURN DURING ELECTROTHERAPY, TWO INCIDENTS REPORTED. PATIENT WAS PROVIDED NEDICAL TREATMENT.
Patient problems: Burn(s)
MAUDE report 23737798 ↗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 ↗InjurySep 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT WAS BURNED DURING ELECTROTHERAPY.
Patient problems: Burn(s)
MAUDE report 23080661 ↗InjuryAug 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE E-STIM THERAPY IS BURNING PATIENTS, PATIENT SUSTAINED A DIME SIZED 2ND DEGREE BURN UNDER ONE ELECTRODE.
Patient problems: Burn(s)
MAUDE report 22929617 ↗InjuryAug 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT SUSTAINED DERMAL BURNS DURING COMBO MODALITY, NO ERROR MESSAGE RECEIVED ON THE DEVICE.
Patient problems: Burn(s)
MAUDE report 22812228 ↗InjuryApr 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT SUSTAINED 5 BURNS WHERE ELECTRODES WERE PLACES DURING TREATMENT THAT WERE TREATED TOPICALLY BY WOUND CARE USING STANDARD BURN CREAM AND INFECTION TREATMENTS.
Patient problems: Burn(s); Unspecified Infection
MAUDE report 21940269 ↗InjuryApr 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT SUSTAINED 2ND DEGREE BURNS UNDER 3 ELECTRODES DURING TREATMENT THAT REQUIRED MEDICAL TREATMENT AT URGENT CARE.
Patient problems: Burn(s)
MAUDE report 21915074 ↗InjuryMar 5, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT THE UNIT HAS BURNED PATIENT DURING INTERFERENTIAL TREATMENT.
Patient problems: Burn(s)
MAUDE report 21532030 ↗InjuryMar 5, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT WAS RECEIVING ELECTRICAL STIMULATION, UPON COMPLETION OF TREATMENT AND INSPECTION OF SKIN AFTER ELECTRICAL STIMULATION. THE PHYSICAL THERAPIST ASSISTANT NOTED SKIN ALTERATIONS AND NOTIFIED THEIR SUPERVISOR OF THE FINDINGS.
Patient problems: Burn(s)
MAUDE report 21532028 ↗InjuryFeb 12, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
THE CLINICIAN REPORTED A SMALL BURN ON THE PATIENT AFTER WHICH THIS UNIT WAS PROMPTLY REMOVED FROM SERVICE.
Patient problems: Burn(s)
MAUDE report 21370553 ↗InjuryFeb 5, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
IT WAS REPORTED THAT THE UNIT HAS GIVEN ELECTRICAL BURNS TO PATIENTS.
Patient problems: Burn(s)
MAUDE report 21317570 ↗InjuryNov 7, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT UNIT ERRORED DURING TREATMENT, THE CLINICIAN WENT TO REMOVE ROPE, BUT IT JERKED BACK INTO THE UNIT PULLING THE DOCTORS ARM AND PATIENTS HEAD.
Patient problems: Insufficient Information
MAUDE report 20627257 ↗
Other Djo, LLC products
All Djo, LLC devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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