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Use caution Drug recall · FDA · Published March 4, 2019

Athleticare Anti-Bacterial Hand Soap Recall: Triclosan Issue

Athleticare recalls Anti-Bacterial Hand Soap AC 550 because it contains triclosan, an ingredient no longer allowed in over-the-counter consumer antiseptic washes.

🇺🇸 FDA recall #D-0994-2019DrugAthleticare ›
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Recalling firmPetra Hygienic Systems Int Ltd86 Moyal Crt · Concord, Canada
✎ GovInfoNow plain-language explainer

Petra Hygienic Systems Int Ltd is recalling Athleticare Anti-Bacterial Hand Soap AC 550 because the product does not meet federal monograph standards. Specifically, it contains triclosan, which is prohibited in over-the-counter consumer antiseptic wash products. The recall covers all lots of this 4-liter bottle size distributed nationwide. Read more at govinfonow.com/recall/39132-athleticare-anti-bacterial-hand-soap-recall-triclosan-issue.

Source Summary by GovInfoNow · govinfonow.com/recall/39132-athleticare-anti-bacterial-hand-soap-recall-triclosan-issue · Updated October 11, 2026 · FDA enforcement record: FDA #D-0994-2019

Cite this page

“Athleticare Anti-Bacterial Hand Soap Recall: Triclosan Issue.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39132-athleticare-anti-bacterial-hand-soap-recall-triclosan-issue. Based on FDA recall #D-0994-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0994-2019%22&limit=1).

The FDA announced on March 4, 2019, that Petra Hygienic Systems Int Ltd voluntarily recalled Athleticare Anti-Bacterial Hand Soap AC 550. The product does not meet the over-the-counter monograph because it contains triclosan, an ingredient no longer permitted in such washes.

How to tell if you have it

  • Brand: Athleticare
  • Product: Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%
  • Size: 4 litres/1.1 US Gallon bottles, packaged in 4 x 4
  • NDC: 42326-550-01
  • UPC: 0 65936 10335 5
  • Distribution: Nationwide in the USA

The hazard

The product does not meet the monograph for over-the-counter consumer antiseptic/antibacterial wash products because it contains triclosan. The FDA stated that this ingredient can no longer be contained in these types of products.

Context

GovInfoNow's records show other recent recalls of similar products include Trifluent Pharma Wound Care Gel Recall (2026-04-08) and ACME Children's Hand Sanitizer Wipes Recall (2026-01-20). Taro Recalls Children's Ibuprofen Due to Foreign Substance occurred on 2026-03-02.

How to tell if you have this one

Look for Athleticare Anti-Bacterial Hand Soap AC 550 in 4-liter (1.1 US gallon) bottles. Check for NDC 42326-550-01 and UPC 0 65936 10335 5. The product was sold nationwide in cases of four bottles.

  • Brand
    Athleticare
  • Product
    ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%, 4 litres/1.1 US Gallon bottles, packaged in 4 x 4
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check your inventory

    Verify if you have Athleticare Anti-Bacterial Hand Soap AC 550 with NDC 42326-550-01 or UPC 0 65936 10335 5.

  2. Monitor for instructions

    The recall record does not specify a remedy, return process, or refund procedure at this time.

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 21 months after the firm started it.

1. Firm started the recall: Mar 4, 201912. FDA classified it Class III: Mar 12, 201923. Published in FDA’s Enforcement Report: Mar 13, 201934. FDA terminated the recall: Dec 10, 2020420192020
  1. Firm started the recall
  2. FDA classified it Class III
  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.

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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-0994-2019 (March 4, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0994-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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