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Ended FDAEvent 99195 (29 days ago)

Wild Coast Brew Loose-Leaf Teas

The Shadow, The Creator, and The Lover loose-leaf teas contain Ashwagandha root, an unsafe food additive.

Recall ended Sep 29, 2026. Still check yours.

Low risk

Eating it is unlikely to cause health problems.

FDA Class III recall · How risk is rated

What to do

What happened

Wild Coast Brew LLC of Coquille, Oregon, recalled The Shadow Loose-Leaf Tea, The Creator Loose-Leaf Tea, and The Lover Loose-Leaf Tea because the dry tea blends contain Ashwagandha root, which is an unsafe food additive. The recall began June 5, 2026, and was added to the FDA's Enforcement Report on September 16, 2026. The products were distributed nationwide.

Summary by Recall Canary from the FDA notice.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is yours affected?

3 products

Match the list below, then check the codes the FDA notice also names.

  1. The Shadow Loose-Leaf Tea - Winter Spice Black Tea, net wt. 2oz (56 g). Product is

    UPC
    • 09122024
    • 10092025
    • 11252025
    • 02172026
  2. The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane, net wt. 1.5oz (42 g). Product is

    UPC
    • 07102025
    • 11052025
    • 11252025
    • 12312025
    • 02262026
  3. The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.5oz (42 g). Product is

    UPC
    • 05222025
    • 06122025
    • 08212025
    • 01222026

From the FDA notice

UPC 00198168252543.

Details

Company began the recall
Sold in

Distributed nationwide.

Event ID
99195
Recall numbers
H-1369-2026 to H-1371-2026
Company
Wild Coast Brew LLCCoquille, Oregon
Recall type
Voluntary: Firm initiated
Customers told by
E-Mail
  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. Listed on Recall Canary

  4. Recall ended

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration