Wild Coast Brew Tart Chocolaty Tisane Recall: Ashwagandha Safety Risk
Wild Coast Brew recalls 1.5oz Tart Chocolaty Tisane due to unsafe Ashw: risk of harm from consuming Ashwagandha root in tea blends.
Recall notice
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
What happened, in plain English
Wild Coast Brew is recalling their Tart Chocolaty Tisane tea because it contains Ashwagandha root, an unsafe food additive. This poses a risk to consumers who may experience health issues from consuming the product. Read more at govinfonow.com/recall/995120-wild-coast-brew-tart-chocolaty-tisane-recall-ashwagandha-safety-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/995120-wild-coast-brew-tart-chocolaty-tisane-recall-ashwagandha-safety-risk · Updated September 23, 2026 · Official notice: FDA #H-1371-2026
Cite this page
“Wild Coast Brew Tart Chocolaty Tisane Recall: Ashwagandha Safety Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/995120-wild-coast-brew-tart-chocolaty-tisane-recall-ashwagandha-safety-risk. Based on FDA recall #H-1371-2026.
Why it’s dangerous
Ashwagandha root is listed as an unsafe food additive in this tea blend. Consuming it could lead to health issues, though the exact risk isn't specified in the recall notice.
Who’s affected
Anyone who purchased the Tart Chocolaty Tisane tea from Wild Coast Brew. People with allergies to Ashwagandha or those with specific health conditions may be at higher risk.
How to tell if you have this one
Check for the product name 'Tart Chocolaty Tisane' with a net weight of 1.5oz (42g). Look for the UPC 00198168682364 or lot codes 05222025, 06122025, 08212025, 01222026.
- Brand
Wild Coast Brew- Product
The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag within- Category
Food
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Completed- Distribution
Distributed nationwide.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| H-1369-2026 | The Shadow Loose-Leaf Tea - Winter Spice Black Tea, net wt. 2oz (56 g). Product is packaged in cellophane bag within tubular container. UPC 00198168252543. Ingredients: Black Tea ( Keemun & Assam), Cinnamon, Holy Basil, Milky Oats, Licorice Root, Ashwagandha, Ginger. Produced By Wild Coast Brew, Myrtle Point, OR.; Lot Codes: 09122024 10092025 11252025 02172026 | 706 pkg. |
| H-1370-2026 | 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 Codes: 07102025 11052025 11252025 12312025 02262026 | 794 pkg. |
| H-1371-2026 | The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag within tubular container. UPC 00198168682364. Ingredients: Hibiscus, Cacao Husks, Oxidized Blackberry Leaf, Raspberry Leaf, Rose, Lemon Peel, Peppermint, Ashwagandha, Tangerine oil. Produced By Wild Coast Brew, Myrtle Point, OR.; Lot Codes: 05222025 06122025 08212025 01222026 | 603 pkg. |
What to do — step by step
Check Product Details
Verify the product name and lot codes to confirm if it's part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Distributed nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 12 days after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class III
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #H-1371-2026 (June 5, 2026)
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.