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Lower risk Medical device recall · FDA · Published December 18, 2017

COACH Self-Adhering Sports Wrap Recall: Natural Latex Allergy Risk

Johnson & Johnson recalls select COACH Self-Adhering Sports Wraps due to potential natural latex allergy from early manufacturing. Affected products may cause allergic reactions in sensitive individuals.

🇺🇸 FDA recall #Z-1201-2018Medical deviceCOACH ›
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Recalling firmJohnson & Johnson Consumer, Inc.199 Grandview Rd · Skillman, NJ 08558-1311
✎ GovInfoNow plain-language explainer

Johnson & Johnson is recalling select COACH Self-Adhering Sports Wraps (2-inch size) because they contain natural latex from early production. This could cause allergic reactions in people sensitive to latex. Read more at govinfonow.com/recall/72294-coach-self-adhering-sports-wrap-recall-natural-latex-allergy-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/72294-coach-self-adhering-sports-wrap-recall-natural-latex-allergy-risk · Updated August 31, 2026 · FDA enforcement record: FDA #Z-1201-2018

Cite this page

“COACH Self-Adhering Sports Wrap Recall: Natural Latex Allergy Risk.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72294-coach-self-adhering-sports-wrap-recall-natural-latex-allergy-risk. Based on FDA recall #Z-1201-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1201-2018%22&limit=1).

The FDA announced on Dec. 18, 2017, that Johnson & Johnson Consumer Inc. is recalling select COACH Self-Adhering Sports Wraps (size: 2in) because the labeling incorrectly states the product is not made with natural rubber latex. The agency classified this as a Class II recall.

How to tell if you have it

  • Brand: COACH
  • Product: Self-Adhering Sports Wrap (size: 2in)
  • UPC: 100497502
  • UPC: 381370079286
  • Lot code: 3813700497530024

The hazard

The recall addresses a labeling error where the product claims not to contain natural rubber latex, despite natural latex being used as a base ingredient in early-stage manufacturing. This discrepancy may reduce the allergic protein found in natural latex, posing a risk to individuals with latex allergies.

Context

GovInfoNow's records show Johnson & Johnson Consumer Inc. has 1 other recall on record since 2021-07-14. On 2021-07-14, the company issued a Neutrogena SPF 100+ Sunscreen Recall for cGMP Deviations. Other recent recalls of similar products include Stryker NICO Myriad Handpieces Recall (2025-10-31), Stryker NICO BrainPath Shephard's Hook Recall (2025-10-31) and Stryker NICO Myriad Illumination Packs (2025-10-31).

How to tell if you have this one

Check for the product code 100497502, 381370079286, or 3813700497530024 on the packaging. The product is a 2-inch size COACH Self-Adhering Sports Wrap.

  • Brand
    COACH
  • Category
    Medical device
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationally
Recall numberProduct, codes & lotsQuantity
Z-1201-2018COACH¿ Self-Adhering Sports Wrap (size: 2in); 100497502 381370079286 3813700497530024—
Z-1202-2018COACH¿ Self-Adhering Sports Wrap (size: 3in); 100497602 381370079293 3813700497600024—
Z-1203-2018Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 2in); 111615000 381371161508 103813711615050000—
Z-1204-2018Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 3in); 111615100 381371161515 103813711615120000—
Z-1205-2018Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 1in); 111614500 381371161454 10381371161451—
Z-1206-2018Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 2in); 111614600 381371161461 103813711614680000—
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product codes 100497502, 381370079286, or 3813700497530024 on the packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationally” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

1. Firm started the recall: Dec 18, 201712. FDA classified it Class II: Mar 27, 201823. Published in FDA’s Enforcement Report: Apr 4, 201834. FDA terminated the recall: Apr 14, 2020420172020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Do I need to stop using these wraps?

No, but people with latex allergies should avoid using them.

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Where this comes from

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-1201-2018 (December 18, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1201-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 31, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA