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Class I: serious health riskTerminated

Fahman Enterprises Pran Spice Powder Turmeric Recall

Pran Spice Powder Turmeric , 14

Fahman Enterprises, Inc · Dallas, TX

Risk level
Class I
Reported by FDA
Jul 30, 2014
Recall ID
F-2223-2014
Check your lot numberHow we source this data

Summary

Fahman Enterprises recalled Pran Spice Powder Turmeric starting Oct 17, 2013. The FDA classified it as Class I (serious health risk) and published enforcement report F-2223-2014 on Jul 30, 2014. Reason: Elevated levels of lead. Status: Terminated.

Why it was recalled

Elevated levels of lead.

Product description

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

Lot numbers, UPCs & expiration codes

Best Before 25 JAN 15

Where it was sold

Dallas, Texas area

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-2223-2014
Classification
Class I
Status
Terminated
Recall initiated
Oct 17, 2013
FDA report date
Jul 30, 2014
Quantity
4 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Fahman Enterprises, Inc

Original FDA data

Every field from FDA enforcement report F-2223-2014, exactly as published.

Show all FDA fields
City
Dallas
State
TX
Status
Terminated
Country
United States
Event ID
66523
Address
10600 Boomer Cir
Address (line 2)
Ste 500
Code information
Best Before 25 JAN 15
Postal code
75238-5362
Report date
Jul 30, 2014
Product type
Food
Recall number
F-2223-2014
Classification
Class I
Recalling firm
Fahman Enterprises, Inc
Product quantity
4 cases
Termination date
Jan 12, 2015
Reason for recall
Elevated levels of lead.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Pran Spice Powder Turmeric , 14.10 oz. (400g) clear plastic laminated pouch, UPC 8 3173000502 3
Distribution pattern
Dallas, Texas area
Recall initiation date
Oct 17, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jul 24, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2223-2014, published Jul 30, 2014. View the source record (openFDA) · FDA enforcement reports

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

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