CLASS II ONGOING Drug recall · Reported 23 Jun 2021 · FDA Enforcement Report
Imperia Elita Vitaccino Coffee sachets, 15 sachets recalled
Dash Xclusive is recalling Imperia Elita Vitaccino Coffee sachets, 15 sachets per, Global Beauty Technologies, distributed nationwide in the US. The recall was initiated on 11 May 2021 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0628-2021
- FDA event ID
- 87923
- Recalling firm
- Dash Xclusive, Glendale, CA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 11 May 2021
- FDA classified
- 11 Jun 2021
- Reported
- 23 Jun 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
Timeline
| 11 May 2021 | Recall initiated by company | |
| 11 Jun 2021 | Classified by FDA | +31 days |
| 23 Jun 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Imperia Elita Vitaccino Coffee, 10 g sachets, 15 sachets per box, Global Beauty Technologies, Manufactured for: Imperia-Elita Ltd. & Co, KG D- 35435 Wettenberg
Where it was distributed
Nationwide within the United States
Questions about this recall
Why was it recalled?
Marketed without an approved NDA/ANDA: FDA analysis determined presence of the pharmaceutical ingredients Sibutramine and Fluoxetine
Which lots are affected?
All Lots
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.