Djo, Llc
Complete recall history across all FDA and CPSC categories — 7 total recalls
Djo, Llc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (7)
FDA medical device enforcement actions by Djo, Llc
| Date | Product | Reason | Class |
|---|---|---|---|
| Sep 25, 2025 | Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02 | The IFU (Information for Use) on the wrap instructs the user to heat the hot ... | Class II |
| Sep 7, 2021 | GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5... | Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may ... | Class I |
| Sep 7, 2021 | Ultra-Myossage Lotion 1-gallon bottle, REF: 4262; Myossage Lotion 1-gallon b... | Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may ... | Class I |
| Jan 17, 2019 | Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expirati... | The product may not meet sterility requirements. Product labeled as sterile, ... | Class II |
| Jun 25, 2018 | This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and... | The device accessories were not labeled with appropriate latex warning. | Class II |
| Aug 21, 2015 | Monode, Shortwave Accessory Model #: 02200002 Used in conjunction with th... | Overheating and burning of the wire insulation inside the applicator. | Class II |
| May 28, 2013 | VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite System... | DJO, LLC has recently identified a product safety issue with the battery asse... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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