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Class II: temporary or reversible health riskTerminated

WS Global Himalayan Pain Relief Tea for Gout and Recall

Himalayan Pain Relief Tea for Gout and Hangover

WS Global Inc · Brooklyn, NY

Risk level
Class II
Reported by FDA
Apr 3, 2024
Recall ID
F-1094-2024
Check your lot numberHow we source this data

Summary

WS Global recalled Himalayan Pain Relief Tea for Gout and starting Dec 13, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1094-2024 on Apr 3, 2024. Reason: Contains undeclared drugs Diclofenac and Dexamethasone Acetate. Status: Terminated.

Why it was recalled

Contains undeclared drugs Diclofenac and Dexamethasone Acetate

Product description

Himalayan Pain Relief Tea for Gout and Hangover

Lot numbers, UPCs & expiration codes

all codes on us market

Where it was sold

nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1094-2024
Classification
Class II
Status
Terminated
Recall initiated
Dec 13, 2023
FDA report date
Apr 3, 2024
Quantity
4000 Units
Recall type
N/A
Recalling firm
WS Global Inc

Original FDA data

Every field from FDA enforcement report F-1094-2024, exactly as published.

Show all FDA fields
City
Brooklyn
State
NY
Status
Terminated
Country
United States
Event ID
93604
Address
156 Flushing Ave Fl 4
Code information
all codes on us market
Postal code
11205-1112
Report date
Apr 3, 2024
Product type
Food
Recall number
F-1094-2024
Classification
Class II
Recalling firm
WS Global Inc
Product quantity
4000 Units
Termination date
Apr 22, 2026
Reason for recall
Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Product description
Himalayan Pain Relief Tea for Gout and Hangover
Distribution pattern
nationwide
Recall initiation date
Dec 13, 2023
Initial firm notification
Press Release
Center classification date
Mar 22, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1094-2024, published Apr 3, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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