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.
“DJO NYLATEX Wrap Accessories: Latex Warning Missing - Recall.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/70747-djo-nylatex-wrap-accessories-latex-warning-missing-recall. Based on FDA recall #Z-2590-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2590-2020%22&limit=1).
DJO, LLC recalled NYLATEX WRAP accessories for Intelect devices because they lacked appropriate latex warnings, the FDA said on June 25, 2018. Owners should contact the company for a remedy.
The NYLATEX WRAP accessories were not labeled with appropriate latex warnings. The wraps are composed of nylon and natural rubber.
Context
GovInfoNow's records show DJO, LLC has issued four other recalls since Jan. 17, 2019. Other recent recalls of similar products include Stryker NICO Myriad Handpieces (Oct. 31, 2025), Stryker NICO BrainPath Shephard's Hook (Oct. 31, 2025) and Stryker NICO Myriad Illumination Packs (Oct. 31, 2025).
How to tell if you have this one
Check for the product names and part numbers listed in the recall notice, such as NYLATEX 4X36 PKG SING FOR UNIT or 10827/ NYLATEX 2-1/2 X 18 CUT. These wraps are accessories for specific Intelect devices.
Brand
DJO
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for the part numbers or product names listed in the recall notice to confirm if your wrap is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 41 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 4.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2590-2020 (June 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2590-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.