Super Herbs 350 mg Recall: Undeclared Sibutramine Hazard
Super Herbs recalls 350 mg capsules due to undeclared sibutramine and phenolphthalein. Class I drug recall affecting all lots.
Stop using this now
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
Contact the company
What happened, in plain English
Super Herbs is recalling its 350 mg supplement, sold in bottles of 30 capsules, because it contains undeclared prescription drugs. The product was marketed without an approved New Drug Application or Abbreviated New Drug Application. It may contain sibutramine, desmethylsibutramine, and/or phenolphthalein. Read more at govinfonow.com/recall/43353-super-herbs-recalls-super-herbs-350-mg-30-capsules-per.
Source Summary by GovInfoNow · govinfonow.com/recall/43353-super-herbs-recalls-super-herbs-350-mg-30-capsules-per · Updated October 11, 2026 · FDA enforcement record: FDA #D-0909-2016
Cite this page
“Super Herbs 350 mg Recall: Undeclared Sibutramine Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43353-super-herbs-recalls-super-herbs-350-mg-30-capsules-per. Based on FDA recall #D-0909-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0909-2016%22&limit=1).
Why it’s dangerous
The supplement contains sibutramine and/or its metabolite desmethylsibutramine, which are prescription drugs not approved for over-the-counter sale. It may also contain phenolphthalein. These undeclared ingredients can cause serious cardiovascular or gastrointestinal issues in users who are unaware they are ingesting medication.
Who’s affected
Consumers who purchased Super Herbs 350 mg capsules in bottles of 30 are at risk. Because the product contains undeclared prescription ingredients, anyone taking it for weight loss or other purposes could experience serious health effects.
How to tell if you have this one
Look for bottles labeled 'Super Herbs 350 mg' containing 30 capsules. The recall covers all lots of this product. Only 9 bottles were distributed to 9 consignees.
- Brand
Super Herbs- Category
Drug
What to do — step by step
Stop taking the supplement
Discontinue use immediately due to the presence of undeclared prescription drugs.
Discard or return the product
Dispose of any remaining capsules or return them to the distributor, as no specific remedy instructions are provided in this record.
How this recall unfolded
Recall timeline
FDA terminated this recall 8.9 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-0909-2016 (November 23, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0909-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.