Wild Coast Brew LLC Recall: Dry tea blends product containing Ashwagandha root which is an unsafe food additive.

🇺🇸 United States

1. June 5, 2026 - Recall initiated
2. June 17, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-1371-2026

Event ID

99195

Status

Completed

Classification

Class III

Company

Wild Coast Brew LLC

Product description

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.

Quantity

603 pkg.

Reason

Dry tea blends product containing Ashwagandha root which is an unsafe food additive.

Recall initiation date

June 5, 2026

Report date

June 17, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Distributed nationwide.

UPC, lot, and code information

UPC 00198168682364; Lot Codes: 05222025 06122025 08212025 01222026

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

October 6, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 99195 with 2 other product entries in Public Health Trace.

Responsible company: Wild Coast Brew LLC

Other recalls from Wild Coast Brew LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: October 6, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Completed." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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