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Unrated Drug recall · FDA · Published February 16, 2022

Sure Unscented Deodorant Aerosol Recall: Benzene Contamination Risk

TCP HRB ACQUISITON LLC recalls Sure Unscented Anti-perspirant Deodorant Aerosol (10% Aluminum Chlorohydrate) due to benzene contamination. All 6 oz cans with NDC 41595-5517-06, expired by August 2023.

🇺🇸 FDA recall #D-0208-2024DrugTCP HRB ACQUISITON LLC ›
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Recalling firmTCP HRB ACQUISITON LLC270 Saugatuck Ave · Westport, CT 06880-6431
✎ GovInfoNow plain-language explainer

What happened, in plain English

TCP HRB ACQUISITON LLC is recalling Sure Unscented Anti-perspirant Deodorant Aerosol cans because they contain benzene, a chemical known to be harmful. This recall affects all 6 oz cans with the specified NDC number and expiration date. Read more at govinfonow.com/recall/35214-sure-unscented-deodorant-aerosol-recall-benzene-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35214-sure-unscented-deodorant-aerosol-recall-benzene-contamination-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0208-2024

Cite this page

“Sure Unscented Deodorant Aerosol Recall: Benzene Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/35214-sure-unscented-deodorant-aerosol-recall-benzene-contamination-risk. Based on FDA recall #D-0208-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0208-2024%22&limit=1).

Why it’s dangerous

Benzene is a chemical that can be harmful when inhaled or absorbed through the skin. The presence of benzene in these deodorant cans poses a health risk, especially with frequent use.

Who’s affected

All owners of the recalled Sure Unscented Anti-perspirant Deodorant Aerosol cans (6 oz, NDC 41595-5517-06) are affected. People using these products regularly are most at risk due to potential benzene exposure.

How to tell if you have this one

Look for 6 oz aerosol cans labeled 'Sure Unscented Anti-perspirant Deodorant' with NDC 41595-5517-06. The product expires by August 2023.

  • Brand
    TCP HRB ACQUISITON LLC
  • Category
    Drug
FDA recall event · 3 products

All 3 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 I
  • Status
    Ongoing
  • Distribution
    Nationwide in the US and Canada
Recall numberProduct, codes & lotsQuantity
D-0207-2024Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA; All lots, expiry on or before August 2023a) 0.4 million cans, b) 3.4 million cans
D-0208-2024Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06; All lots, expiry on or before August 20230.5 million
D-0209-2024Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06; All lots, expiry on or before August 20235.4 million
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product label for the NDC number 41595-5517-06 and expiration date by August 2023.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

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 US and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 23 months after the firm started it.

1. Firm started the recall: Feb 16, 202212. FDA classified it Class I: Dec 28, 202323. Published in FDA’s Enforcement Report: Jan 3, 2024320222024
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

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

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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-0208-2024 (February 16, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0208-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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