Medical DeviceMay 20, 2026
DONJOY ICEMAN W/,UNIV,LOOP,NS,EH recall — FDA Z-2136-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Recall history in this database
Classification mix: Class II: 7, Class I: 2.
Medical DeviceMay 20, 2026
DONJOY ICEMAN CLASSIC CUBE recall — FDA Z-2134-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Medical DeviceMay 20, 2026
DONJOY ICEMAN W/,UNIV,LOOP,NS,RH recall — FDA Z-2135-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Medical DeviceMay 20, 2026
DONJOY ICEMAN, W/COLDPAD, NS, RH recall — FDA Z-2137-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Medical DeviceDec 3, 2025
DJO Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02 recall — FDA Z-0722-2026
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…
Class IIFDA: OngoingDJO, LLC
Medical DeviceOct 13, 2021
DJO Ultra-Myossage Lotion 1-gallon bottle, REF: 4262 recall — FDA Z-0010-2022
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…
Class IFDA: OngoingDJO, LLC
Medical DeviceOct 13, 2021
DJO GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 recall — FDA Z-0009-2022
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…
Class IFDA: OngoingDJO, LLC
Medical DeviceJul 22, 2020
DJO This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic recall — FDA Z-2590-2020
The device accessories were not labeled with appropriate latex warning.
Class IIFDA: TerminatedDJO, LLC
Medical DeviceJul 24, 2019
DJO Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date recall — FDA Z-1985-2019
The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
Class IIFDA: OngoingDJO, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies DJO, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.