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Stop using now Drug recall · FDA · Published January 16, 2020

Shandex Acne Cleansing Bar Recall: Metal Contaminant Hazard

Walgreens recalls Shandex Acne Cleansing Bar (10% Benzoyl Peroxide) due to visible metal contaminants from manufacturing. Consumers should stop using affected bars immediately.

🇺🇸 FDA recall #D-0822-2020DrugShandex ›
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Recalling firmShandex Personal Care Manufacturing Inc.5 Herriott St · Perth, Canada
✎ GovInfoNow plain-language explainer

Walgreens is recalling Shandex Acne Cleansing Bar products that contain visible metal contaminants from manufacturing. This hazard could cause injury if the metal particles enter the skin. Read more at govinfonow.com/recall/37406-shandex-acne-cleansing-bar-recall-metal-contaminant-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/37406-shandex-acne-cleansing-bar-recall-metal-contaminant-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #D-0822-2020

Cite this page

“Shandex Acne Cleansing Bar Recall: Metal Contaminant Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37406-shandex-acne-cleansing-bar-recall-metal-contaminant-hazard. Based on FDA recall #D-0822-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0822-2020%22&limit=1).

Shandex Personal Care Manufacturing Inc. recalled Walgreens Acne Cleansing Bar with benzoyl peroxide 10% on Jan. 16, 2020, after the Food and Drug Administration announced the presence of a metal contaminant. The FDA issued the recall under number D-0822-2020.

How to tell if you have it

  • Brand: Shandex
  • Product: Walgreens Acne Cleansing Bar, Benzoyl Peroxide 10%, NET WT 4 oz (113 g)
  • NDC: 0363-0137-11
  • Lot #: L 19173
  • Expiration: 06/20/2021
  • Quantity: 20,448 cartons

The hazard

The product contains a visible metal contaminant identified as screen wire from the manufacturing process. The FDA classified this Class II recall as voluntary and initiated by the firm.

Context

GovInfoNow's records show other recent recalls of similar products include Merck Noxafil Powdermix Recall (2025-12-12) with metal particulates risk, Trifluent Pharma Wound Care Gel Recall (2026-04-08) for contaminated product from a shared facility, and Guardian Drug Goodsense Ultra Strength Antacid Tablets Recall (2026-05-28) involving metallic particles hazard.

How to tell if you have this one

Check for the product name 'Acne Cleansing Bar', NDC code 0363-0137-11, lot number L 19173, and expiration date of June 2021. The product is sold by Walgreens and comes in 4 oz bars.

  • Brand
    Shandex
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using It Now

    Immediately stop using the recalled Shandex Acne Cleansing Bar product if you have it.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Jan 16, 202012. FDA classified it Class II: Jan 30, 202023. Published in FDA’s Enforcement Report: Feb 5, 202034. FDA terminated the recall: Nov 6, 202042020
  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.

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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-0822-2020 (January 16, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0822-2020 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