FDA Drug recall D-0020-2017
Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada…
- FDA Drug
- Class I
- terminated
- Published 2016-10-19
On 2016-10-19 the FDA classified a Class I recall of Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada… by Bee Xtreme, citing marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0020-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-12-23 |
| Published | 2016-10-19 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Bee Xtreme |
| Distribution | n/a |
Product
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
Reason
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Identifiers
| code_info | All Lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0020-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.