Class IITerminated in FDA datasetRecall initiated Aug 26, 2025

Mai Tai 20mg Gummies Brand Name: None - unlabeled bulk (private-label consignee) Generic Name:…

Recalling firm: Extract Labs, Inc.

Why it was recalled

Potential peanut protein cross-contact.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 30, 2025.

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Compare the exact product and package details with the label you have.

ProductMai 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)
Package size5kg

FDA code information

Lot: 25JD042507A EXP: 07/2027 Printed on bulk bag identifier adhesive

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Full FDA record and distribution details

Original 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)

Extracted codes and context

TypeCode / valueContext
lot25JD042507ALot: 25JD042507A EXP: 07/2027 Printed on bulk bag identifier adhesive

Original FDA recall reason

Potential peanut protein cross-contact.

Recall details

Recall number
H-0624-2025
Event ID
97500
FDA status
Terminated
Initiated
Aug 26, 2025
Reported
Oct 1, 2025
Classified
Sep 22, 2025
Terminated
Oct 30, 2025
Quantity
19,750 gummies
Location
Lafayette, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.

FDA source record · H-0624-2025

Data updated September 16, 2026. View official FDA data ↗

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