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This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NY...

FDA Device Recall #Z-2590-2020 — Class II — June 25, 2018

Recall Summary

Recall Number Z-2590-2020
Classification Class II — Moderate risk
Date Initiated June 25, 2018
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm DJO, LLC
Location Vista, CA
Product Type Devices
Quantity 41,801 units

Product Description

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.

Reason for Recall

The device accessories were not labeled with appropriate latex warning.

Distribution Pattern

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 and WV The countries of Algeria, Armenia, Australia, Austria, Azerbaijan, Bahamas, Bahrain, Belgium, Bolivia, Brazil, Bulgaria, Canada, Chile, China, Colombia, Congo, Congo, The Democratic Republic of the, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, England, Estonia, Ethiopia, Finland, France, Germany, Greece, Guatemala, Hong Kong, Iceland, India, Indonesia, Iran, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kenya, Korea, Republic of, Kuwait, Lebanon, Lithuania, Luxembourg, Malaysia, Malta, Mexico, Morocco, Netherlands, Norway, Oman, Pakistan, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Tanzania, United Republic of, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Viet Nam.

Lot / Code Information

Part Number/ Description: 10679/ NYLATEX 4X36 PKG SING FOR UNIT 10827/ NYLATEX 2-1/2 X 18 CUT 10828/ NYLATEX 2-1/2X18 SEWN 10829/ NYLATEX 2-1/2X36 CUT 10830/ NYLATEX 2-1/2X36 SEWN 10831/ NYLATEX 2-1/2X48 CUT 10832/ NYLATEX 2-1/2X48 SEWN 10833/ NYLATEX 4X18 CUT 10834/ NYLATEX 4X18 SEWN 10835/ NYLATEX 4X36 CUT 10836/ NYLATEX 4X36 SEWN 10837/ NYLATEX 4X48 CUT 10838/ NYLATEX 4X48 SEWN 10839/ NYLATEX 6X18 CUT 10840/ NYLATEX 6X18 SEWN 10841/ NYLATEX 6X36 CUT 10842/ NYLATEX 6X36 SEWN 10843/ NYLATEX 6X48 CUT 10844/ NYLATEX 6X48 SEWN 12-0248-8/ NYLATEX 2-1/2X24 CUT 1210CHT/ NYLATEX 4X36 BAG OF 3 1214CHT/ NYLATEX 6X18 BAG OF 3 1213CHT/ NYLATEX 4X60 BAG OF 3 19991/ NYLATEX 6X60 CUT 19992 /NYLATEX 6X60 SEWN 19993/ NYLATEX 4X60 CUT 19994/ NYLATEX 4X60 SEWN 25-10648/ NYLATEX 2-1/2X24 25-10679/ NYLATEX 4X36 12-10648/ NYLATEX 2-1/2 X 24 SEWN 12-8655/ ASSY,STIM MODULE CH 3/4 INT'L PKG 3448274/ C-5 220-240V OEM ENRAF W/PKS 2778-10/ INTELECT MOBILE COMBO, INT'L STD, 10CM APPL 2777/ INTELECT MOBILE 2CH STIMINT'L STD 2778/ INTELECT MOBILE COMBO, INT'L STD, 5CM APPL 2778-2/ INTELECT MOBILE COMBO, INT'L STD, 2CM APPL 5951/ INTELECT VITALSTIM 2 CHANNEL THERAPY SYSTEM, INT'L STD 2752CC/ INT ADV 2CH COLOR COMBO INT'L STD 2762CC/ INT ADV 2CH COLOR COMBO, INT'L 5CM APPL 2772MC/ INT ADVANCED COMBO MONOCHROMEINT'L STD 2755CS/ INT ADV 2CH COLOR STIM INT'L STD 2762CC-2/ INT ADV 2CH COLOR COMBO W/O EM INT'L STD, 2CM APPL 2765CS/ INT ADV 2CH COLOR STIM W/EMG INTL STD 2773MS/ INT ADVANCED STIM MONOCHROME INT'L STD 2762CC-10/ INT ADV 2CH COLOR COMBO W/O EM INT'L STD, 10CM APPL 2770/ STIM MODULE CH 3/4 INT'L PKG 3102/ C-5 120V PKG A 3114/ C-5 220V PKG A INT'L STD 1200/ NYLATEX INTRO PACK 1202/ NYLATEX 2-1/2X18 BAG OF 3* 1204/ NYLATEX 2-1/2X36 BAG OF 3* 1206/ NYLATEX 2-1/2X48 BAG OF 3* 1208/ NYLATEX 4X18 BAG OF 3* 1210/ NYLATEX 4X36 BAG OF 3* 1212/ NYLATEX 4X48 BAG OF 3* 1213/ NYLATEX 4X60 BAG OF 3* 1214/ NYLATEX 6X18 BAG OF 3* 1216/ NYLATEX 6X36 BAG OF 3* 1218/ NYLATEX 6X48 BAG OF 3* 1219/ NYLATEX 6X60 BAG OF 3 1264/ NYLATEX 2-1/2X24 BAG OF 3* 10648/ NYLATEX 2-1/2X24 SEWN 28099/ KIT, LEAD IN MOBILE STIM INTL 59048/ KIT LEAD STIM INT CLINIC VITLS (CH 1/2) 27378/ KIT LEAD INT ADVANCED 2CH 27509/ KIT LED 4CH EPR INT L

Other Recalls from DJO, LLC

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Z-0722-2026 Class II Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, ... Sep 25, 2025
Z-0010-2022 Class I Ultra-Myossage Lotion 1-gallon bottle, REF: 42... Sep 7, 2021
Z-0009-2022 Class I GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/... Sep 7, 2021
Z-1985-2019 Class II Aircast REF 3011 - PL RX only VF-PL Sterile Cuf... Jan 17, 2019
Z-0121-2016 Class II Monode, Shortwave Accessory Model #: 02200002 ... Aug 21, 2015

Frequently Asked Questions

Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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