Bee Xtreme Recalls Oasis Supplements Due to Hidden Drugs
Bee Xtreme recalls 732 bottles of Oasis dietary supplement capsules. The FDA found they contain sibutramine and phenolphthalein, posing serious health risks.
Stop using this now
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
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What happened, in plain English
Bee Xtreme is recalling all lots of its Oasis Dietary Supplement Capsules (500 mg, 45 count) because the products were marketed without an approved New Drug Application. FDA analysis determined that the capsules contain sibutramine and phenolphthalein, which are not permitted in dietary supplements. This constitutes a Class I recall, indicating a situation where there is a reasonable probability that the product will cause serious adverse health consequences or death. Read more at govinfonow.com/recall/43307-bee-xtreme-recalls-oasis-supplements-due-to-hidden-drugs.
Source Summary by GovInfoNow · govinfonow.com/recall/43307-bee-xtreme-recalls-oasis-supplements-due-to-hidden-drugs · Updated October 11, 2026 · FDA enforcement record: FDA #D-0020-2017
Cite this page
“Bee Xtreme Recalls Oasis Supplements Due to Hidden Drugs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43307-bee-xtreme-recalls-oasis-supplements-due-to-hidden-drugs. Based on FDA recall #D-0020-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0020-2017%22&limit=1).
Why it’s dangerous
The product contains sibutramine and phenolphthalein. Sibutramine is a drug ingredient that was withdrawn from the market due to cardiovascular risks, and phenolphthalein is a laxative ingredient banned for use in over-the-counter drugs due to cancer concerns. Ingesting these substances poses a significant health risk.
Who’s affected
Consumers who purchased Oasis Dietary Supplement Capsules from any source are at risk. Because the distribution pattern is listed as unknown, it is unclear exactly where or when these bottles were sold, so anyone with this specific supplement should assume they may be affected.
How to tell if you have this one
Look for bottles of Oasis Dietary Supplement Capsules, 500 mg, in 45-count packaging. The product was manufactured for Timeless Solutions at 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, and distributed by BeeXtreme LLC in Punxsutawney, PA. All lots are included in this recall.
- Brand
Bee Xtreme- 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 I- Status
Terminated- Distribution
Unknown
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0019-2017 | La' Trim Plus Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA; All Lots | 589 bottles |
| D-0020-2017 | Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA; All Lots | 732 bottles |
| D-0021-2017 | Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA; All Lots | 13 bottles |
What to do — step by step
Stop using the product
Do not consume any remaining capsules from the recalled Oasis Dietary Supplement bottles.
Dispose of the product
Discard the recalled supplement bottles immediately to prevent accidental ingestion by others.
How this recall unfolded
Recall timeline
FDA terminated this recall 13 months 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-0020-2017 (December 23, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0020-2017 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.