Class IITerminatedVoluntary: Firm initiated
Extract Labs, Inc.: food recall H-0621-2025
Extract Labs, Inc. of Lafayette, CO recalled Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg… Reason: Potential peanut protein cross-contact. The FDA listed it as Class II in its Enforcement Report dated Oct 1, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Oct 30, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- 2180 gummies (109/20 ct bottles)
- Reason for recall
- Potential peanut protein cross-contact.
- Codes, lots and dates on the package
- Lot: 25E5082907A (we call this a batch ID) EXP: 07/2027 Printed on the bottom of the bottle
- Distribution pattern
- Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.
- Recalling firm
- Extract Labs, Inc., Lafayette, CO
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 26, 2025 |
| Classified by the FDA | Sep 22, 2025 |
| Published in the Enforcement Report | Oct 1, 2025 |
| Terminated | Oct 30, 2025 |
Other products in the same recall event
The FDA groups related products under one recall event (event 97500).
- H-0624-2025 — 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…
- H-0623-2025 — 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…
- H-0622-2025 — 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…
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0621-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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