The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag with
Summary
The FDA issued a Class III for The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net wt. 1.5oz (42 g). Pr by Wild Coast Brew LLC. Reason: Dry tea blends product containing Ashwagandha root which is an unsafe food additive..
Details
Source
Food Recall
External ID
H-1370-2026
Action Date
2026-06-17
Status
Completed
Category
food
Product Description
The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag within tubular container. UPC 00198168088265. Ingredients: Oxidized Fireweed, Coriander Seed, Lemongrass, Peppermint, Ginger, Coconut Flakes, Lemon Peel, Ashwagandha, Calendula, Red Pepper Flakes. Produced by Wild Coast Brew, Myrtle Point, OR.
Lot/Code Info: Lot Codes: 07102025 11052025 11252025 12312025 02262026
Quantity Affected: 794 pkg.
Reason for Recall
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
Distribution
Distributed nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-05
Company
Coquille, OR
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 193 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Wild Coast Brew LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wild Coast Brew LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wild Coast Brew LLC have FDA actions?
Wild Coast Brew LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1370-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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