DJO, LLC recalls
Every recall we track for DJO, LLC — 9 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
9 recalls since 2017. 22% rated “stop using now”.
All FDA recall records for DJO, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 1 | 0 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 1 | 0 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 4 | 0 | 4 |
What to do if you have a recalled DJO, LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All DJO, LLC recalls
5 shown- Lower riskMedical device
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product
DONJOY recalls ICEMAN cold therapy units with model 11-1424 due to a broken connector that may interrupt prescribed cold therapy. Affected units were sold starting May 2023. Consumers should contact DONJOY for a repair or replacement.
DONJOYMar 19, 2026 - Stop using nowMedical device
DJO, LLC recalls Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
DJO recalls back and shoulder cold wraps that may leak or burn if heated in microwave. Affected models include DP163CT02 and DP163CT03. Stop using immediately to avoid second-degree burns.
DJOSep 25, 2025 - Use cautionMedical device
DJO, LLC recalls Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon bottle, REF: 4210, located in the following
DJO recalls 1-gallon Ultra-Myossage Lotion bottles (REFs 4262 and 4210) due to potential bacterial contamination. FDA issued a warning on August 18, 2021.
DJOSep 7, 2021 - Lower riskMedical device
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 recalls Aircast REF 3011 sterile cuff packages (Lot #418003) due to potential failure to meet sterility standards. This affects medical use items sold through specific channels.
DJOJan 17, 2019 - Lower riskMedical device
DJO, LLC recalls This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product
DJO recalls NYLATEX wrap accessories for Intelect devices due to missing latex allergy warnings. These wraps contain natural rubber and may cause allergic reactions if not properly labeled.
DJOJun 25, 2018
DJO, LLC recall questions
How many recalls has DJO, LLC had?
9 recalls from DJO, LLC are on record with U.S. safety agencies, from 2018–2026.
What is the most recent DJO, LLC recall?
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product, dated Mar 19, 2026. Every DJO, LLC recall is listed on this page, newest first.
What should I do if I have a recalled DJO, LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new DJO, LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.