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RECALL RECORD — CLASS IRecall completedD-0266-2022/FDA enforcement
American Screening LLC·Cosmetics·Nov 19, 2021

Americanscreening Hand Sanitizer (Ethyl Alcohol 70%) Antimicrobial Formula Vitamin E &…

What you need to know

Class I

  • What happened

    Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall completed · classified by the FDANationwide (US)More cosmetics

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Product identification

Source: FDA COSMETICS

Brand nameAmerican Screening LLC
Recalling firmAmerican Screening LLCShreveport, LA, United States
UPC / barcodes
8 40050 51579 2
Lot / date codes
  • Black capped bottles have no lot numbers but include expiration dates of 5/21/2022 and 05/24/2022. Clear capped bottles have neither lot numbers nor expiration dates.
Distribution area
Nationwide

Distributed Nationwide in the USA

United States

Quantity affected153, 336 bottles
Recall initiationFDA report date: December 15, 2021
FDA recall numberD-0266-2022

Beyond the headline

The recall, in context

American Screening LLC initiated this cosmetics recall on November 19, 2021. The FDA enforcement report states: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles. The FDA report lists distribution as: Distributed Nationwide in the USA.

The FDA enforcement report describes the reason as: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

Americanscreening Hand Sanitizer (Ethyl Alcohol 70%) Antimicrobial Formula Vitamin E &… was made or distributed by American Screening LLC in Shreveport, LA, United States. This page reflects FDA report D-0266-2022, dated December 15, 2021.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Americanscreening Hand Sanitizer (Ethyl Alcohol 70%) Antimicrobial Formula Vitamin E &… recall?

American Screening LLC recalled Americanscreening Hand Sanitizer (Ethyl Alcohol 70%) Antimicrobial Formula Vitamin E &… in an FDA Class I enforcement action reported as D-0266-2022. Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the American Screening LLC recall still active?

The FDA lists this recall as recall completed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-0266-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.