H-0623-2025 Class II Terminated

Recalled by Extract Labs, Inc. — Lafayette, CO

FDA food recall H-0623-2025 was initiated by Extract Labs, Inc. on Aug 26, 2025 and is designated Class II. Reason for recall: Potential peanut protein cross-contact. The recall status is terminated (terminated Oct 30, 2025). Affected quantity: 19,810 gummies.

Recall Details

Product Type
Food
Report Date
Oct 1, 2025
Initiation Date
Aug 26, 2025
Termination Date
Oct 30, 2025
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
19,810 gummies

Product Description

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)

Reason for Recall

Potential peanut protein cross-contact.

Distribution Pattern

Product distributed throughout the United States and Australia, Germany, United Kingdom, Malaysia, and New/Zealand.

Code Information

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

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for H-0623-2025
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for H-0623-2025. Report a data issue: hello@regdatalab.com.