CHATTANOOGA 2872Recalls & reported problems
Djo, LLC · VECTRA GEN 2C COMBO W/O EMG PK US STD · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00888912296854), received between Aug 26, 2016 and May 23, 2024 — classified as 3 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Burn(s)2
- Chest Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMay 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT WAS BURNED DURING TREATMENT.
Patient problems: Burn(s)
MAUDE report 19388697 ↗InjuryMay 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT WAS BURNED DURING TREATMENT.
Patient problems: Burn(s)
MAUDE report 19388696 ↗InjuryAug 26, 2016Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
COMPLAINT RECEIVED THAT ALLEGES "PATIENT TAKEN TO THE ER DUE TO CHEST PAINS THAT BEGAN DURING TREATMENT". QUESTIONNAIRE WAS RECEIVED FROM CUSTOMER OR CLINICIAN. TREATMENT WAS INTERRUPTED, PROGRESS TOWARDS RECOVERY WAS NOT IMPEDED. PATIENT REQUESTED TREATMENT STOP WHEN FEELING CHEST PAINS APPROXIMATELY ONE MINUTE INTO TREATMENT, VITALS WERE WNL, WAS TRANSPORTED TO ER FOR EVALUATION. DEVICE NOT RETURNED TO MANUFACTURER FOR EVALUATION.
Patient problems: Chest Pain
MAUDE report 5908286 ↗
Other STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT devices
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- CHATTANOOGA 2760Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT15 reports
- CHATTANOOGA 2783Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT9 reports
- CHATTANOOGA 2763Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT6 reports
- CHATTANOOGA 2792Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2798Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 4738Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
- CHATTANOOGA 2796Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.