DJO recalls
DJO has 11 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 20 May 2026. 8 are still ongoing. 5 were reported in the last 12 months. The most frequent reason is device malfunction.
Total recalls11since 2013
Last 12 months5reported
Class I218% of total
Ongoing8latest 20 May 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 18%Class II 9 82%Class III 0 0%
Why djo is recalled
Product types
By year
Ongoing djo recalls
8 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Donjoy Iceman, W/coldpad, Ns, Rh recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Donjoy Iceman W/,univ,loop,ns,rh recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Donjoy Iceman Classic Cube recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Donjoy Iceman W/,univ,loop,ns,eh recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Cold Form Wrap: Back recalled by DJO | DJO | Packaging Defects | Nationwide |
| Device | CLASS I | GEL Conductor, Description recalled by DJO | DJO | Other | Nationwide |
All djo recalls, newest first
11 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Donjoy Iceman, W/coldpad, Ns, Rh recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Donjoy Iceman W/,univ,loop,ns,rh recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Donjoy Iceman Classic Cube recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Donjoy Iceman W/,univ,loop,ns,eh recalled by DJO | DJO | Device Malfunction | Nationwide |
| Device | CLASS II | Cold Form Wrap: Back recalled by DJO | DJO | Packaging Defects | Nationwide |
| Device | CLASS I | GEL Conductor, Description recalled by DJO | DJO | Other | Nationwide |
| Device | CLASS I | Ultra-Myossage Lotion recalled by DJO | DJO | Other | Nationwide |
| Device | CLASS II | This is an accessory to Intelect Advanced, Intelect Mobile recalled | DJO | Foreign Material | Nationwide |
| Device | CLASS II | Aircast REF 3011 - PL RX only Vf-pl Sterile Cuff Pkg recalled by DJO | DJO | Sterility | OK |
| Device | CLASS II | Monode, Shortwave Accessory recalled by DJO | DJO | Other | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.