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Class II: temporary or reversible health riskTerminated

Sazon Bohio with Coriander and Annatto Recall

Sazon Bohio with Coriander and Annatto

Sazon, Inc. · Doral, FL

Risk level
Class II
Reported by FDA
May 13, 2015
Recall ID
F-2192-2015
Check your lot numberHow we source this data

Summary

Sazon recalled Sazon Bohio with Coriander and Annatto starting Jan 26, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2192-2015 on May 13, 2015. Reason: Cumin used has undeclared peanut protein. Status: Terminated.

Why it was recalled

Cumin used has undeclared peanut protein.

Product description

Sazon Bohio with Coriander and Annatto

Lot numbers, UPCs & expiration codes

UPC 7639820011, Lots: 601095 and 601105, 6.33 oz.

Where it was sold

US- NY, TX, FL, PA, PR, IL, VA, MA

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-2192-2015
Classification
Class II
Status
Terminated
Recall initiated
Jan 26, 2015
FDA report date
May 13, 2015
Quantity
672
Recall type
Voluntary: Firm initiated
Recalling firm
Sazon, Inc.

Original FDA data

Every field from FDA enforcement report F-2192-2015, exactly as published.

Show all FDA fields
City
Doral
State
FL
Status
Terminated
Country
United States
Event ID
70750
Address
2000 Nw 92nd Ave
Code information
UPC 7639820011, Lots: 601095 and 601105, 6.33 oz.
Postal code
33172-2928
Report date
May 13, 2015
Product type
Food
Recall number
F-2192-2015
Classification
Class II
Recalling firm
Sazon, Inc.
Product quantity
672
Termination date
Jan 24, 2017
Reason for recall
Cumin used has undeclared peanut protein.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Sazon Bohio with Coriander and Annatto
Distribution pattern
US- NY, TX, FL, PA, PR, IL, VA, MA
Recall initiation date
Jan 26, 2015
Initial firm notification
E-Mail
Center classification date
May 6, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2192-2015, published May 13, 2015. View the source record (openFDA) · FDA enforcement reports

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

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