Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 26, 2025 (14 months ago)

Mai Tai 20mg Gummies Brand Name recall

Recalled by Extract Labs, Inc. · Lafayette, CO, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential peanut protein cross-contact.

See the recall's own reason text for the specifics. All other reasons recalls.

What 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)

Quantity: 19,750 gummies

Food: Chocolate & candy Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Nationwide.

FDA's distribution note: Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Extract Labs, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 26, 2025
In FDA report of
Oct 1, 2025
Terminated
Oct 30, 2025
FDA recall number
H-0624-2025 · event 97500
Official record
FDA enforcement report search

Also recalled with it (3 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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