Class IITerminated in FDA datasetRecall initiated Aug 26, 2025

Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement…

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.

ProductSugar-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
Package size3.53oz
UPC850029647928

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC850029647928er 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
lot25E5082907ALot: 25E5082907A (we call this a batch ID) EXP: 07/2027 Printed on the bottom of the bottle

Original FDA recall reason

Potential peanut protein cross-contact.

Recall details

Recall number
H-0621-2025
Event ID
97500
FDA status
Terminated
Initiated
Aug 26, 2025
Reported
Oct 1, 2025
Classified
Sep 22, 2025
Terminated
Oct 30, 2025
Quantity
2180 gummies (109/20 ct bottles)
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-0621-2025

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

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