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ACTIVE RECALL — CLASS IIActive recallD-0628-2021/FDA enforcement
Dash Xclusive·Cosmetics·May 11, 2021

Imperia Elita Vitaccino Coffee, 10 g Sachets, 15 Sachets Per Box, Global Beauty Technologies, …

What you need to know

Class II

  • What happened

    Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine

  • 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.

Active recall · classified by the FDANationwide (US)More cosmetics

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Product identification

Source: FDA COSMETICS

Brand nameDash Xclusive
Recalling firmDash XclusiveGlendale, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • All Lots
Distribution area
Nationwide

Nationwide within the United States

United States

Quantity affected25 pieces (boxes containing 15 sachets)
Recall initiationFDA report date: June 23, 2021
FDA recall numberD-0628-2021

Beyond the headline

The recall, in context

Dash Xclusive initiated this cosmetics recall on May 11, 2021. The FDA enforcement report states: Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine. The FDA report lists distribution as: Nationwide within the United States.

The FDA enforcement report describes the reason as: Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine

Imperia Elita Vitaccino Coffee, 10 g Sachets, 15 Sachets Per Box, Global Beauty Technologies, … was made or distributed by Dash Xclusive in Glendale, CA, United States. This page reflects FDA report D-0628-2021, dated June 23, 2021.

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 Imperia Elita Vitaccino Coffee, 10 g Sachets, 15 Sachets Per Box, Global Beauty Technologies, … recall?

Dash Xclusive recalled Imperia Elita Vitaccino Coffee, 10 g Sachets, 15 Sachets Per Box, Global Beauty Technologies, … in an FDA Class II enforcement action reported as D-0628-2021. Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine

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 Dash Xclusive recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-0628-2021. 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.