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Class II: temporary or reversible health riskTerminated

Daaks International Fenugreek Recall

Fenugreek, 3 dozen per case

Daaks International · Los Angeles, CA

Risk level
Class II
Reported by FDA
Oct 31, 2012
Recall ID
F-0517-2013
Check your lot numberHow we source this data

Summary

Daaks International recalled Fenugreek starting Feb 13, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0517-2013 on Oct 31, 2012. Reason: DAAKS International is recalling fenugreek because it contains the toxic weed Senecio vulgaris. Status: Terminated.

Why it was recalled

DAAKS International is recalling fenugreek because it contains the toxic weed Senecio vulgaris.

Product description

Fenugreek, 3 dozen per case.

Lot numbers, UPCs & expiration codes

not availble

Where it was sold

California, Washington

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-0517-2013
Classification
Class II
Status
Terminated
Recall initiated
Feb 13, 2012
FDA report date
Oct 31, 2012
Quantity
388 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Daaks International

Original FDA data

Every field from FDA enforcement report F-0517-2013, exactly as published.

Show all FDA fields
City
Los Angeles
State
CA
Status
Terminated
Country
United States
Event ID
63341
Address
945 Birch St
Code information
not availble
Postal code
90021-2311
Report date
Oct 31, 2012
Product type
Food
Recall number
F-0517-2013
Classification
Class II
Recalling firm
Daaks International
Product quantity
388 cases
Termination date
Oct 30, 2012
Reason for recall
DAAKS International is recalling fenugreek because it contains the toxic weed Senecio vulgaris.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Fenugreek, 3 dozen per case.
Distribution pattern
California, Washington
Recall initiation date
Feb 13, 2012
Initial firm notification
Letter
Center classification date
Oct 25, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0517-2013, published Oct 31, 2012. View the source record (openFDA) · FDA enforcement reports

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

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