Class IITerminated in FDA datasetAug 26, 2025

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…

Recalling firm: Extract Labs, Inc.

Why it was recalled

Potential peanut protein cross-contact.

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

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

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

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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.