PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported October 1, 2025

Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Mai Tai: 24 bags x 5kg and 1 bag x 4kg UPC:

Potential peanut protein cross-contact.

Recall #
H-0624-2025
Affected scope
19,750 gummies
Initiated
August 26, 2025
Compiled from official public sources by the editorial team.
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Extract Labs, Inc. recalled Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic … - a moderate-severity action.

Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic … was recalled by Extract Labs, Inc. in October 1, 2025. Reason: Potential peanut protein cross-contact.. Check the official notice for the remedy. Verify recall #H-0624-2025 with the FDA Food before acting.

The recall

Extract Labs, Inc. issued this moderate-severity FDA Food recall-Potential peanut protein cross-contact..

Moderate
severity level
Class II
classification
October 1, 2025
reported

Sourced from official FDA Food enforcement records. Verify recall #H-0624-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #H-0624-2025) was formally reported on October 1, 2025, with the manufacturer initiating the action on August 26, 2025. It is classified under Moderate severity (Class II), with a current status of Terminated. Extract Labs, Inc. is listed as the recalling firm, operating out of Lafayette, CO. Federal records list the affected scope as 19,750 gummies.

The documented reason for this recall is: Potential peanut protein cross-contact. Distribution data in the federal record shows the product reached: Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.. Distribution scope 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.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,002 dietary supplements recalls on record

-1000100200300400 20072010201320162019202220252026 9
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.

Severity

Moderate

Affected scope

19,750 gummies

Related Recalls

6

6 from same agency

Product description

Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Mai Tai: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)

Reason for recall

Potential peanut protein cross-contact.

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 H-0624-2025
Date reported October 1, 2025
Date initiated August 26, 2025
Recalling firm Extract Labs, Inc.
Firm location Lafayette, CO
Affected scope 19,750 gummies
Distribution Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.

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

What to do with this recall

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

  • Check the recall number (H-0624-2025) 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?
Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name: Dietary Supplement Strength: 20mg CBD and 20mg D9 THC per gummy Dosage: Not declared at bulk stage (consignee determines serving size) Form: Gummy Administration: Oral Intended use: Dietary supplement for further packaging/labeling by consignee Type of packaging: Shipped in poly gusset bags, inside corrugated brown boxes, no consumer label applied. Net wt. Mai Tai: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label). Recalled by Extract Labs, Inc.. Units affected: 19,750 gummies.
Why was this product recalled?
Potential peanut protein cross-contact.
Which agency issued this recall?
This recall was issued by the FDA Food on October 1, 2025. Severity: Moderate. Recall number: H-0624-2025.
Where was the recalled product distributed?
Distribution: Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand..
How do I check if my product is affected by a recall?
Check the product description and recall number (H-0624-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported October 1, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.