Recall events
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Event 73167
Event summary
Timeline bucket December 23, 2015
Product types Drug
Classifications Class I
Statuses Terminated
Recalling firm wording Bee Xtreme
Dossier provenance
Source snapshots represented here
openFDA Drug Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
3 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
drug · product 1 of 3
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
D-0019-2017
Recall number D-0019-2017
Initiated December 23, 2015
Classification Class I
Status Terminated
Quantity 589 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Distribution pattern Unknown
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[8618]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 3
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
D-0020-2017
Recall number D-0020-2017
Initiated December 23, 2015
Classification Class I
Status Terminated
Quantity 732 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Distribution pattern Unknown
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[8739]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 3
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
D-0021-2017
Recall number D-0021-2017
Initiated December 23, 2015
Classification Class I
Status Terminated
Quantity 13 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein
Distribution pattern Unknown
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[8689]
FDA event record
· Exact recall-number query on openFDA
