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Class II: temporary or reversible health riskTerminated

Shakti Group Cumin Ground Product of India 50 lbs C/7784 Recall

Cumin Ground Product of India 50 lbs C/7784

SHAKTI GROUP USA LLC · New Brunswick, NJ

Risk level
Class II
Reported by FDA
Dec 9, 2015
Recall ID
F-0339-2016
Check your lot numberHow we source this data

Summary

Shakti Group recalled Cumin Ground Product of India 50 lbs C/7784 starting Aug 25, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0339-2016 on Dec 9, 2015. Reason: Cumin contains 8.0 ppm peanut allergen. Status: Terminated.

Why it was recalled

Cumin contains 8.0 ppm peanut allergen.

Product description

Cumin Ground Product of India 50 lbs C/7784

Lot numbers, UPCs & expiration codes

Lot 55968

Where it was sold

NY

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-0339-2016
Classification
Class II
Status
Terminated
Recall initiated
Aug 25, 2015
FDA report date
Dec 9, 2015
Quantity
39,450 lbs
Recall type
Voluntary: Firm initiated
Recalling firm
SHAKTI GROUP USA LLC

Original FDA data

Every field from FDA enforcement report F-0339-2016, exactly as published.

Show all FDA fields
City
New Brunswick
State
NJ
Status
Terminated
Country
United States
Event ID
72295
Address
14 van Dyke Ave
Code information
Lot 55968
Postal code
08901-3253
Report date
Dec 9, 2015
Product type
Food
Recall number
F-0339-2016
Classification
Class II
Recalling firm
SHAKTI GROUP USA LLC
Product quantity
39,450 lbs
Termination date
Jun 19, 2017
Reason for recall
Cumin contains 8.0 ppm peanut allergen.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Cumin Ground Product of India 50 lbs C/7784
Distribution pattern
NY
Recall initiation date
Aug 25, 2015
Initial firm notification
Letter
Center classification date
Dec 2, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0339-2016, published Dec 9, 2015. View the source record (openFDA) · FDA enforcement reports

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

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