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Lower risk Drug recall · FDA · Published November 20, 2019

Idelle Labs SURE 48 hr Confidence Deodorant Recall: Undeclared Active Ingredient

Idelle Labs recalls SURE 48 hr Confidence Unscented invisible solid deodorant due to undeclared active ingredient. Consumers should check product labels and contact the company for details.

🇺🇸 FDA recall #D-0783-2020DrugIdelle Labs ›
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Contact the company

Recalling firmIdelle LabsOne Helen Of Troy Plaza · El Paso, TX 79912
✎ GovInfoNow plain-language explainer

Idelle Labs is recalling SURE 48 hr Confidence Unscented invisible solid deodorant because it contains an active ingredient not listed on the label. This could lead to unexpected reactions or health issues if the product is used without knowing the full ingredients. Read more at govinfonow.com/recall/37681-idelle-labs-sure-48-hr-confidence-deodorant-recall-undeclared-active.

Source Summary by GovInfoNow · govinfonow.com/recall/37681-idelle-labs-sure-48-hr-confidence-deodorant-recall-undeclared-active · Updated October 5, 2026 · FDA enforcement record: FDA #D-0783-2020

Cite this page

“Idelle Labs SURE 48 hr Confidence Deodorant Recall: Undeclared Active Ingredient.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37681-idelle-labs-sure-48-hr-confidence-deodorant-recall-undeclared-active. Based on FDA recall #D-0783-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0783-2020%22&limit=1).

The FDA announced on Nov. 20, 2019, that Idelle Labs voluntarily recalled SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant because the label lists an active ingredient not present in the product.

How to tell if you have it

  • Brand: Idelle Labs
  • Product: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g)
  • NDC#: 41595-5509-2
  • UPC: 8 83484 71717 2
  • Lots: 19273K1, 19274K1, 19274K2, 19725K1, 19725K2, 19726K1
  • Distribution: Nationwide in the USA

The hazard

According to the FDA, the product contains an undeclared active ingredient because the ingredient listed on the label is not the actual active ingredient in the product.

Context

GovInfoNow's records show other recent recalls of similar products include CoValence Laboratories Remedy Gel Hydrocortisone 1% Recall (2026-03-18), Gold Star Deodorant Recall (2025-12-26), and Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21).

How to tell if you have this one

Check for the product name 'SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant' with the lot numbers 19273K1, 19274K1, 19274K2, 19725K1, 19725K2, or 19726K1. The product was made in Canada and distributed by Idelle Labs, Ltd. in El Paso, TX.

  • Brand
    Idelle Labs
  • Product
    SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC
  • Category
    Drug
FDA recall event · 4 products

All 4 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 III
  • Status
    Terminated
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lots
D-0783-2020SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912; Lots: 19273K1, 19274K1, 19274K2, 19725K1, 19725K2, 19726K1
D-0784-2020SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant Net Wt 2.6 oz (73g) NDC# 41595-5547-1 UPC 8 83484 31020 5 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912; Lot: 19277K1
D-0785-2020SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5514-1 UPC 8 83484 717936 6 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912; Lots: 19279K1, 19279K2, 19280K1
D-0786-2020SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt 2.7 oz (76g) NDC# 41595-5513-2 UPC 8 83484 71794 3 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912; Lots: 19277K2, 19278K1
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot numbers 19273K1, 19274K1, 19274K2, 19725K1, 19725K2, or 19726K1 on the product label.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.9 years after the firm started it.

1. Firm started the recall: Nov 20, 201912. Published in FDA’s Enforcement Report: Jan 15, 202023. FDA classified it Class III: Jan 16, 202034. FDA terminated the recall: Sep 28, 2022420192022
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class III
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from this product?

The recall is for potential skin irritation or allergic reactions, not serious injury. The danger level is low risk.

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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 #D-0783-2020 (November 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0783-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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