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Lower risk Drug recall · FDA · Published November 19, 2021

American Screening Hand Sanitizer Recall: Water Bottle-Looking Containers

American Screening recalls 8 fl oz hand sanitizer bottles that look like water bottles. These containers may confuse consumers with drinking water bottles, leading to accidental ingestion. Stop using and check for black or clear caps.

🇺🇸 FDA recall #D-0266-2022DrugAmerican Screening ›
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Contact the company

Recalling firmAmerican Screening LLC9742 Saint Vincent Ave Ste 100 · Shreveport, LA 71106-7129
✎ GovInfoNow plain-language explainer

American Screening is recalling hand sanitizer bottles that resemble drinking water bottles. This could lead to accidental ingestion if consumers mistake them for water bottles. Read more at govinfonow.com/recall/35528-american-screening-hand-sanitizer-recall-water-bottle-looking-containers.

Source Summary by GovInfoNow · govinfonow.com/recall/35528-american-screening-hand-sanitizer-recall-water-bottle-looking-containers · Updated August 18, 2026 · FDA enforcement record: FDA #D-0266-2022

Cite this page

“American Screening Hand Sanitizer Recall: Water Bottle-Looking Containers.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35528-american-screening-hand-sanitizer-recall-water-bottle-looking-containers. Based on FDA recall #D-0266-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0266-2022%22&limit=1).

The FDA announced on Nov. 19, 2021, that American Screening LLC voluntarily recalled its AmericanScreening hand sanitizer because the packaging resembles drinking water bottles. The agency classified the recall as Class I.

How to tell if you have it

  • AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL)
  • UPC 8 40050 51579 2
  • UPC 00840050515792

The hazard

The hand sanitizer is packaged in containers that resemble drinking water bottles, creating a risk of accidental ingestion. The FDA issued this recall to address the labeling issue.

Context

GovInfoNow's records show other recent recalls include the Baxter Sterile Water for Irrigation Recall on Dec. 22, 2025, and the Zep Alcohol Sanitizer Spray Recall on May 22, 2026. The American Regent ACETYLCYSTEINE Solution Recall occurred on July 24, 2026.

How to tell if you have this one

Check for bottles with either a black or clear top. Black capped bottles have expiration dates of 5/21/2022 or 05/24/2022. Clear capped bottles have no lot numbers or expiration dates.

  • Brand
    American Screening
  • Product
    AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL)
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Bottle Type

    Look for bottles with black or clear tops. Black capped bottles have expiration dates of 5/21/2022 or 05/24/2022.

  2. Stop Using if Confused

    If you mistake the bottle for a water bottle, stop using it immediately.

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: “Distributed 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 published this recall 26 days after the firm started it.

1. Firm started the recall: Nov 19, 202112. FDA classified it Class I: Dec 6, 202123. Published in FDA’s Enforcement Report: Dec 15, 202132021
  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-0266-2022 (November 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0266-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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