Djo, Llc
3300 Eagle Parkway, Fort Worth, TX, US
Registered product codes
3 product codes
Recent MDR events
961 on file
- AIRCASTJul 21, 2026InjuryMW5190947
- DONJOYJul 14, 2026Injury9616086-2026-00026
- DONJOYJul 6, 2026Injury9616086-2026-00025
- CMFJun 17, 2026Injury9616086-2026-00024
- CHATTANOOGAMay 31, 2026Injury9616086-2026-00023
- DONJOY ECONOMY WRAP AROUND HINGEMay 20, 2026Malfunction25229068
- CHATTANOOGAMay 20, 2026Injury9616086-2026-00021
- DRYTEX ECONOMY HINGE KNEE, WRAP, POP, XSMay 6, 2026Malfunction25092930
- DR COMFORTMay 6, 2026Injury9616086-2026-00018
- LIGHTFORCEMay 6, 2026Injury9616086-2026-00016
Recalls
11 on file
- Open, ClassifiedMay 8, 2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
View FDA record ↗ - Open, ClassifiedMay 8, 2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
View FDA record ↗ - Open, ClassifiedMay 8, 2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
View FDA record ↗ - Open, ClassifiedMay 8, 2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
View FDA record ↗ - Open, ClassifiedNov 26, 2025
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures capable of causing a second degree burn.
View FDA record ↗ - TerminatedJul 13, 2020
The device accessories were not labeled with appropriate latex warning.
View FDA record ↗ - TerminatedOct 15, 2015
Overheating and burning of the wire insulation inside the applicator.
View FDA record ↗ - TerminatedJul 3, 2013
DJO, LLC has recently identified a product safety issue with the battery assembly for the VenaFlow 30B-B and 30 BI-B products. There is a potential for battery leakage which could result in thermal meltdown (fire).
View FDA record ↗ - Open, ClassifiedUnknown
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
View FDA record ↗ - Open, ClassifiedUnknown
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
View FDA record ↗
Compliance history
Matched by FEI 3014694377.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.