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Food FDA Class II Terminated Undeclared allergen

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 inne

Extract Labs, Inc. Published Oct 1, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 55/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Extract Labs, Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Potential peanut protein cross-contact.

Hazards

Peanuts · primary

Affected products (1)

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

2180 gummies (109/20 ct bottles)

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

Affected areas

Nationwide

Timeline

  1. Initiated
    Aug 26, 2025
  2. Published
    Oct 1, 2025
  3. Terminated
    Oct 30, 2025
Recall number
H-0621-2025
Agency
U.S. Food and Drug Administration
Country
US

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.