CLASS II Food recall · Reported 3 Apr 2024 · FDA Enforcement Report
Himalayan Pain Relief Tea for Gout and Hangover recalled by WS Global
WS Global is recalling Himalayan Pain Relief Tea for Gout and Hangover, distributed nationwide in the US. The recall was initiated on 13 Dec 2023 and the FDA has classified it as Class II.
Check your package
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-1094-2024
- FDA event ID
- 93604
- Recalling firm
- WS Global, Brooklyn, NY
- Brand
- Himalayan Pain
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 13 Dec 2023
- FDA classified
- 22 Mar 2024
- Reported
- 3 Apr 2024
- Type
- N/A
- Customers notified by
- Press Release
- Reason category
- Undeclared Allergens
- Product category
- Tea
Timeline
| 13 Dec 2023 | Recall initiated by company | |
| 22 Mar 2024 | Classified by FDA | +100 days |
| 3 Apr 2024 | Published 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
Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Himalayan Pain Relief Tea for Gout and Hangover
Where it was distributed
nationwide
Questions about this recall
Why was it recalled?
Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Which lots are affected?
all codes on us market
Where was it sold?
nationwide
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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