Dream Body Extreme Gold Recall: Undeclared Sibutramine Hazard
Dream Body Weight Loss recalls Dream Body Extreme Gold capsules due to undeclared sibutramine. Check your bottle for the plastic screw-top cap and all lots.
Stop using this now
Marketed without an approved NDA/ANDA: Undeclared sibutramine.
Contact the company
What happened, in plain English
Dream Body Weight Loss is recalling Dream Body Extreme Gold 800 mg capsules because they are marketed without an approved New Drug Application or Abbreviated New Drug Application. The product contains undeclared sibutramine, a prescription weight-loss drug that was withdrawn from the U.S. market due to safety concerns. All lots of this product sold in the United States are affected. Read more at govinfonow.com/recall/42560-dream-body-extreme-gold-recall-undeclared-sibutramine-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/42560-dream-body-extreme-gold-recall-undeclared-sibutramine-hazard · Updated October 9, 2026 · FDA enforcement record: FDA #D-0106-2017
Cite this page
“Dream Body Extreme Gold Recall: Undeclared Sibutramine Hazard.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42560-dream-body-extreme-gold-recall-undeclared-sibutramine-hazard. Based on FDA recall #D-0106-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0106-2017%22&limit=1).
Why it’s dangerous
The product contains undeclared sibutramine, which poses health risks because its safety profile led to its withdrawal from the U.S. market. Taking an unapproved drug with unknown dosage and purity can lead to serious cardiovascular or other adverse effects not monitored by standard pharmaceutical regulations.
Who’s affected
Consumers who purchased Dream Body Extreme Gold 800 mg capsules, specifically those with a plastic screw-on top bottle, anywhere in the United States.
How to tell if you have this one
Look for a plastic bottle with a screw-on top containing 30 capsules labeled 'Dream Body Extreme Gold 800 mg'. The recall applies to all lots of this specific product distributed in the United States.
- Brand
Dream Body Weight Loss- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
United States
| Recall number | Product, codes & lots |
|---|---|
| D-0106-2017 | Dream Body Extreme Gold 800 mg 30 capsules in a plastic screw on top bottle; All lots. |
| D-0107-2017 | Dream Body 450 mg 30 capsules in a plastic screw on top bottle; All lots. |
| D-0108-2017 | Dream Body Advanced 400 mg 30 capsules in brown foil packets.; All lots. |
What to do — step by step
Stop taking the product
Cease consumption of Dream Body Extreme Gold 800 mg capsules immediately due to the presence of undeclared sibutramine.
Discard or return the item
The record does not specify a return address or disposal method, so you should dispose of it safely away from children and pets.
How this recall unfolded
Recall timeline
FDA terminated this recall 5.2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0106-2017 (July 1, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0106-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.