CHATTANOOGA 42209Recalls & reported problems
Djo, LLC · DURA-STICK PREM 5CM SQUARE 4/PK · 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 00888912341073), received between Aug 20, 2019 and Aug 20, 2019 — 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
- Skin Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 20, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT EXPERIENCED AN ALLERGIC REACTION TO THE ELECTRODES. BETAMETHASONE CREAM WAS PRESCRIBED TO TREAT THE PATIENT. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Skin Irritation
MAUDE report 8909883 ↗
Other ELECTRODE, CUTANEOUS devices
- BIS 186-0106Covidien LP · Electrode, Cutaneous1 death105 reports
- RD SedLine 4248Masimo Corporation · ELECTRODE, CUTANEOUS86 reports
- Cadwell Disposable Ground Electrodes 302288-000Cadwell Industries, Inc. · ELECTRODE, CUTANEOUS1 recall0 reports
- NeuroPlus™ A10042-10Graphic Controls Acquisition Corp · Electrode, Cutaneous32 reports
- BIS 186-0200Covidien LP · Electrode, Cutaneous5 reports
- Rhythmlink® DC2415Rhythmlink International, LLC · Electrode, Cutaneous2 reports
- BioWave Silver Back BioWrap S/M BWRPSILVER-BACK-SMBiowave Corporation · Electrode, Cutaneous2 reports
- Bio-Logic Algo Supplies 011445Natus Medical Incorporated · Electrode, Cutaneous2 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page