Recall Register

Food recall: The Shadow Loose-Leaf Tea - Winter Spice Black Tea, net wt. 2oz (56 g). Product is packaged in cellophane bag within…

Class III FDA enforcement event 99195. Recall start date: . Status in the FDA record: Completed.

Reason for recall, in the words of FDA

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

Class III, in the words of FDA

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

Wild Coast Brew LLC started this food recall on 5 Jun 2026. The firm address in the FDA record is in Coquille, OR. FDA put the recall in Class III. FDA event 99195 has 3 product records. The first FDA enforcement report date is 17 Jun 2026. The record gives the status Completed.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Distributed nationwide.

Recalling firm

Wild Coast Brew LLC, Coquille, OR.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

3 product records in the event.

FDA event 99195: product records
Recall numberProductQuantityClassStatusReport date
H-1369-2026The 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.706 pkg.Class IIICompleted17 Jun 2026
H-1370-2026The 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.…794 pkg.Class IIICompleted17 Jun 2026
H-1371-2026The 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…603 pkg.Class IIICompleted17 Jun 2026

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class III: The lowest of the three FDA recall classes.

The event in context

Food events that started in 2026
304
Share of these events in Class III
7%
Product records in this event
3
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 99195. https://recallregister.com/fda/iii/99195/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Distributed nationwide.
What quantity of product is in FDA event 99195?
The event has 3 product records. The first record gives this quantity: 706 pkg.
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2026 have the same class?
7% of the 304 food events that started in 2026 are in Class III.