CHATTANOOGA 2792Recalls & reported problems
Djo, LLC · VECTRA GENISYS 2CH COMBO, US STD W/CART · Class 2
- 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 00888912294447), received between Mar 5, 2025 and Mar 5, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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. 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 Problem1
- Patient Device Interaction Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
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 ↗
Other STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT devices
- CHATTANOOGA 2738Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT16 reports
- 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 2872Djo, LLC · STIMULATOR, ULTRASOUND AND MUSCLE, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT3 reports
- 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.