Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The device accessories were not labeled with appropriate...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact DJO, LLC directly.
Affected Products
This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product Usage: are intended to be used based on the devices associated with them. Nylatex wraps are composed of nylon and natural rubber and are accessories used to secure electrodes or thermal therapy to a patient.
Quantity: 41,801 units
Why Was This Recalled?
The device accessories were not labeled with appropriate latex warning.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About DJO, LLC
DJO, LLC has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report