CLASS II Food recall · Reported 31 Oct 2012 · FDA Enforcement Report

Fenugreek, 3 dozen recalled by Daaks International

Daaks International is recalling Fenugreek, 3 dozen, distributed in California, Washington. The recall was initiated on 13 Feb 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesnot availble
Quantity recalled388 cases

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-0517-2013
FDA event ID
63341
Recalling firm
Daaks International, Los Angeles, CA
Classification
Class II
Status
Terminated
Recall initiated
13 Feb 2012
FDA classified
25 Oct 2012
Reported
31 Oct 2012
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Other

Timeline

13 Feb 2012Recall initiated by company
25 Oct 2012Classified by FDA+255 days
31 Oct 2012Published in enforcement report+6 days

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

Reason for recall

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

Product as listed by the FDA

Fenugreek, 3 dozen per case.

Where it was distributed

California, Washington

CaliforniaWashington

Questions about this recall

Is Fenugreek, 3 dozen recalled?

Yes. Daaks International recalled Fenugreek, 3 dozen on 13 Feb 2012. The recall is Class II and its status is Terminated. Recall number F-0517-2013.

Why was it recalled?

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

Which lots are affected?

not availble

Where was it sold?

California, Washington

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 21 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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