Food recall

Extract Labs, Inc. recall: Sugar-free Mixed Berry Gummies Brand Name

Extract Labs, Inc., of Lafayette, CO, recalled Sugar-free Mixed Berry Gummies Brand Name and 3 other products. The FDA's reason: “Potential peanut protein cross-contact.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on August 26, 2025, and the FDA first listed it in its Enforcement Report of October 1, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

See FDA's words below

Status

Terminated

Closed October 30, 2025

The recall

Company
Extract Labs, Inc. (Lafayette, CO)
Reason, in FDA's words
“Potential peanut protein cross-contact.”
Where it was sold
Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97500

The 4 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0621-2025 Class II

    Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9 THC per gummy Dosage: 1 gummy Form: Gummy Administration: Oral Intended use: Dietary Supplement Type of packaging: 225cc amber packer bottle with child-resistant cap and inner pressure seal Net wt: 3.53oz UPC: 850029647928 Firm name & address: Extract Labs, Inc., 1399 Horizon Ave, Lafayette, CO 80026

    Codes: Lot: 25E5082907A (we call this a batch ID) EXP: 07/2027 Printed on the bottom of the bottle

    Quantity: 2180 gummies (109/20 ct bottles)

  • H-0622-2025 Class II

    Elderberry 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. Elderberry: 24 bags x 5kg and 1 bag x 3.6kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)

    Codes: Lot: 25JD072107A EXP: 07/2027 Printed on bulk bag identifier adhesive

    Quantity: 19,720 gummies

  • H-0623-2025 Class II

    Blue Razz 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. Blue Razz: 24 bags x 5kg and 1 bag x 4kg UPC: N/A (unlabeled bulk) Firm name & address: None (no consumer label)

    Codes: Lot: 25JD082307A EXP: 07/2027 Printed on bulk bag identifier adhesive

    Quantity: 19,810 gummies

  • H-0624-2025 Class II

    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)

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

    Quantity: 19,750 gummies

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 1, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.