CLASS I Food recall · Reported 30 Jul 2014 · FDA Enforcement Report

Pran Spice Powder Turmeric recalled by Fahman Enterprises

Fahman Enterprises is recalling Pran Spice Powder Turmeric, distributed in Texas. The recall was initiated on 17 Oct 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest Before 25 JAN 15
Quantity recalled4 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-2223-2014
FDA event ID
66523
Recalling firm
Fahman Enterprises, Dallas, TX
Brand
Pran
Classification
Class I
Status
Terminated
Recall initiated
17 Oct 2013
FDA classified
24 Jul 2014
Reported
30 Jul 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Lead & Heavy Metals
Product category
Spices

Timeline

17 Oct 2013Recall initiated by company
24 Jul 2014Classified by FDA+280 days
30 Jul 2014Published 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

Elevated levels of lead.

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

Pran Spice Powder Turmeric , 14.10 oz. (400g) clear plastic laminated pouch, UPC 8 3173000502 3

Where it was distributed

Dallas, Texas area

Texas

Questions about this recall

Why was it recalled?

Elevated levels of lead.

Which lots are affected?

Best Before 25 JAN 15

Where was it sold?

Dallas, Texas area

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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