CLASS I Food recall · Reported 31 Jan 2024 · FDA Enforcement Report

Tapee Tea recalled by The Wiedemann Company

The Wiedemann Company is recalling Tapee Tea, distributed in Florida. The recall was initiated on 8 Nov 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot No. 40-2-00658-2-0012 Best By 10/08/2025
Quantity recalled3600 packs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0775-2024
FDA event ID
93413
Recalling firm
The Wiedemann Company, Louisville, KY
Brand
Tapee
Classification
Class I
Status
Terminated
Recall initiated
8 Nov 2023
FDA classified
19 Jan 2024
Reported
31 Jan 2024
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Packaging Defects
Product category
Tea

Timeline

8 Nov 2023Recall initiated by company
19 Jan 2024Classified by FDA+72 days
31 Jan 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Samples confirm presence of dexamethasone and piroxicam

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Tapee Tea packaged in paper packets - 5 packets per bag

Where it was distributed

Product was distributed to at least OH, FL and possibly other states. Waiting on complete Consignee List.

Florida

Questions about this recall

Why was it recalled?

Samples confirm presence of dexamethasone and piroxicam

Which lots are affected?

Lot No. 40-2-00658-2-0012 Best By 10/08/2025

Where was it sold?

Product was distributed to at least OH, FL and possibly other states. Waiting on complete Consignee List.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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