ModerateClass IITerminated

FDA Food recall · Reported December 20, 2023

TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, FRUIT PUNCH, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Kratom Leaf Extract (30%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583622, POWERED BY LGNDS, 12 bottles of 2oz each per case.

Q: Which agency issued this recall?

This recall was issued by the FDA Food on December 20, 2023. Severity: Moderate. Recall number: F-0505-2024.

Q: Where was the recalled product distributed?

Distribution: U.S. distribution only..

Q: What are the health risks of consuming a recalled food product?

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.

Recall #: F-0505-2024
Affected scope: 15,000 units of 2oz each
Initiated: October 13, 2023

Compiled from official public sources by the publisher. · Updated September 2026

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Lgnds LLC recalled TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, FRUIT PUNCH, 2oz (60ml), Supplement Facts, Ka… - a moderate-severity action.

TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, FRUIT PUNCH, 2oz (60ml), Supplement Facts, Ka… was recalled by Lgnds LLC in December 20, 2023. Reason: Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority lett…. Check the official notice for the remedy. Verify recall #F-0505-2024 with the FDA Food before acting.

The recall

Lgnds LLC issued this moderate-severity FDA Food recall-Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority lett….

Moderate
severity level: 15K units
affected scope: Class II
classification: December 20, 2023
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0505-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, FRUIT PUNCH, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Kratom Leaf Extract (30%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583622, POWERED BY LGNDS, 12 bottles of 2oz each per case.

Reason for recall

Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-0505-2024
Date reported	December 20, 2023
Date initiated	October 13, 2023
Recalling firm	Lgnds LLC
Firm location	Miami, FL
Affected scope	15,000 units of 2oz each
Distribution	U.S. distribution only.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

15,000 units of 2oz each units affected - limited or regional distribution scale.

Regional (<10K units) -

Multi-state (10K – 100K units) ✓ This recall

Large-scale (100K – 1M units) -

Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-0505-2024) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.

Which agency issued this recall? ▼

This recall was issued by the FDA Food on December 20, 2023. Severity: Moderate. Recall number: F-0505-2024.

Where was the recalled product distributed? ▼

Distribution: U.S. distribution only..

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

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Similar Food · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported December 20, 2023. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026