Bee Xtreme Oasis Dietary Supplement Capsules Recall: FDA Class I

Why it was recalled

Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein

Product description

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

Lot numbers, UPCs & expiration codes

All Lots

Where it was sold

Unknown

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-0020-2017
Classification: Class I
Status: Terminated
Recall initiated: Dec 23, 2015
FDA report date: Oct 19, 2016
Quantity: 732 bottles
Recall type: Voluntary: Firm initiated
Recalling firm: Bee Xtreme

Original FDA data

Every field from FDA enforcement report D-0020-2017, exactly as published.

Show all FDA fields

City: Punxsutawney
State: PA
Status: Terminated
Country: United States
Event ID: 73167
Address: 506 N Penn St
Code information: All Lots
Postal code: 15767-1527
Report date: Oct 19, 2016
Product type: Drugs
Recall number: D-0020-2017
Classification: Class I
Recalling firm: Bee Xtreme
Product quantity: 732 bottles
Termination date: Jan 30, 2017
Reason for recall: Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Voluntary / mandated: Voluntary: Firm initiated
Product description: 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
Distribution pattern: Unknown
Recall initiation date: Dec 23, 2015
Initial firm notification: E-Mail
Center classification date: Oct 12, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0020-2017, published Oct 19, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

Bee Xtreme Oasis Dietary Supplement Capsules Recall

Summary