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RECALL RECORD — CLASS IIRecall closedF-1466-2020/FDA enforcement
Sundial Herbal Products·Cosmetics·Jun 30, 2020

"Sundial***traditional Herbal Products***traditional Organic Herbs***mojo Bush***1 Oz.***uses: …

What you need to know

Class II

  • What happened

    Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 closed · classified by the FDANYMore cosmetics

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameSundial Herbal Products
Recalling firmSundial Herbal ProductsBronx, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
Distribution area
NY

NY

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: September 9, 2020
FDA recall numberF-1466-2020

Beyond the headline

The recall, in context

Sundial Herbal Products initiated this cosmetics recall on June 30, 2020. The FDA enforcement report states: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims. The FDA report lists distribution as: NY.

The FDA enforcement report describes the reason as: Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

"Sundial***traditional Herbal Products***traditional Organic Herbs***mojo Bush***1 Oz.***uses: … was made or distributed by Sundial Herbal Products in Bronx, NY, United States. This page reflects FDA report F-1466-2020, dated September 9, 2020.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 lot and date codes 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 "Sundial***traditional Herbal Products***traditional Organic Herbs***mojo Bush***1 Oz.***uses: … recall?

Sundial Herbal Products recalled "Sundial***traditional Herbal Products***traditional Organic Herbs***mojo Bush***1 Oz.***uses: … in an FDA Class II enforcement action reported as F-1466-2020. Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

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 Sundial Herbal Products recall still active?

The FDA lists this recall as recall closed. 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 F-1466-2020. 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

Brand history

More recalls by Sundial Herbal Products

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"Sundial***traditional Herbal Products***traditional Organic Herbs***dog Blood***1 Oz.***uses: …

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

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