DJO Recalls
11 recalls on record · July 10, 2013 to May 20, 2026 · Medical Devices
Recalls by year
13
15
19
20
21
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software Version: No Produc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Produc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Number: 11-1422 Software Version: no Produc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Desc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
December 3, 2025Medical DevicesFDA
DJO, LLC recalls Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
Hazard: 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.
October 13, 2021Medical DevicesFDA
DJO, LLC recalls Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following
Hazard: 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.
October 13, 2021Medical DevicesFDA
DJO, LLC recalls GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO
Hazard: 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.
July 22, 2020Medical DevicesFDA
DJO, LLC recalls This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product Us
Hazard: The device accessories were not labeled with appropriate latex warning.
July 24, 2019Medical DevicesFDA
DJO, LLC recalls Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO
Hazard: The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
October 21, 2015Medical DevicesFDA
DJO, LLC recalls Monode, Shortwave Accessory Model #: 02200002 Used in conjunction with the Intelect Shortwave Diathermy 100 and Inte
Hazard: Overheating and burning of the wire insulation inside the applicator.
July 10, 2013Medical DevicesFDA
DJO, LLC recalls VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite System is a compression pump used for the prevent
Hazard: 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).