CLASS I Drug recall · Reported 16 Apr 2014 · FDA Enforcement Report
Dream Body Slimming Capsule (Chinese bitter orange recalled
Slim Beauty USA is recalling Dream Body Slimming Capsule (Chinese bitter orange 24%, Cassia Seed 18%, Aloe 16%, Lotus, distributed nationwide in the US. The recall was initiated on 10 Dec 2013 and the FDA has classified it as Class I.
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-1222-2014
- FDA event ID
- 67260
- Recalling firm
- Slim Beauty USA, Kearney, NE
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 10 Dec 2013
- FDA classified
- 7 Apr 2014
- Reported
- 16 Apr 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
Timeline
| 10 Dec 2013 | Recall initiated by company | |
| 7 Apr 2014 | Classified by FDA | +118 days |
| 16 Apr 2014 | Published in enforcement report | +9 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: The product contains undeclared sibutramine and . Sibutramine is not currently marketed in the United States, making this product an unapproved new drug.
Product as listed by the FDA
Dream Body Slimming Capsule (Chinese bitter orange 24%, Cassia Seed 18%, Aloe 16%, Lotus Leaf Extract 12%, Medical Amylum 30%), 350 mg, 30-count bottles, Made in China (Beijing).
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and . Sibutramine is not currently marketed in the United States, making this product an unapproved new drug.
Which lots are affected?
Lot # 20130328, Exp 3/27/15
Where was it sold?
Nationwide
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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.
Other products in this recall event
2 other products · FDA event 67260This product is part of a recall event; the main page for the event is Magic Slim capsules (Ling Zhi, Ebony, Fox-nut, Tuckahoe recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Magic Slim capsules (Ling Zhi, Ebony, Fox-nut, Tuckahoe recalled | Slim Beauty USA | Labeling Errors | Nationwide | |
| CLASS I | Dr. Ming's Chinese Capsule (Ginger 50 mg recalled by Slim Beauty U | Slim Beauty USA | Labeling Errors | Nationwide |
More recalls from Slim Beauty USA
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Dr. Ming's Chinese Capsule (Ginger 50 mg recalled by Slim Beauty U | Slim Beauty USA | Labeling Errors | Nationwide |
| Drug | CLASS I | Magic Slim capsules (Ling Zhi, Ebony, Fox-nut, Tuckahoe recalled | Slim Beauty USA | Labeling Errors | Nationwide |