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Class I: serious health riskTerminated

Del Monte Fresh Produce North America Mango Recall

Mango (Fresh Cut): Del Monte brand slices, 32 oz

Del Monte Fresh Produce North America, Inc · Dallas, TX

Risk level
Class I
Reported by FDA
Jul 17, 2013
Recall ID
F-1610-2013
Check your lot numberHow we source this data

Summary

Del Monte Fresh Produce North America recalled Mango starting Sep 20, 2012. The FDA classified it as Class I (serious health risk) and published enforcement report F-1610-2013 on Jul 17, 2013. Reason: In cooperation with the FDA's warning to not consume mangoes from Agricola Daniella in Mexico, Del Monte Fresh Produce N.A., Inc, is initiating a voluntary recall of 1,600 bowls of fresh-cut mangoes distributed to retail outlets due to the potential risk that the mangoes may contain Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frai. Status: Terminated.

Why it was recalled

In cooperation with the FDA's warning to not consume mangoes from Agricola Daniella in Mexico, Del Monte Fresh Produce N.A., Inc, is initiating a voluntary recall of 1,600 bowls of fresh-cut mangoes distributed to retail outlets due to the potential risk that the mangoes may contain Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frai

Product description

Mango (Fresh Cut): Del Monte brand slices, 32 oz., UPC 7-62357-07532-1, 32 oz., UPC 7-17524 72503-5; 16 oz., UPC 7-17524-71902-7, 8 oz., UPC 7-17524-72506-7, UPC 7-17524-72506-6; Del Monte brand chunks, 7 oz., 7 Eleven brand chunks, 6 oz., UPC 0-52548-52070-0

Lot numbers, UPCs & expiration codes

Del Monte, 32 oz., best by 9/26/12, 9/27/12 and 9/28/12; 16 oz., best by 9/26/12 and 9/27/12; 8 oz., best by 9/26/12; chunks 7 oz., Lot 05262101 7 Eleven chunks, 6 oz., best by 9/28/12 and 9/29/12

Where it was sold

Product was distributed directly to the states of Florida, Georgia, Missouri, North Carolina, Ohio, and Texas. Product was then shipped further from the firm's direct accounts.

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-1610-2013
Classification
Class I
Status
Terminated
Recall initiated
Sep 20, 2012
FDA report date
Jul 17, 2013
Quantity
3071 unit total
Recall type
Voluntary: Firm initiated
Recalling firm
Del Monte Fresh Produce North America, Inc

Original FDA data

Every field from FDA enforcement report F-1610-2013, exactly as published.

Show all FDA fields
City
Dallas
State
TX
Status
Terminated
Country
United States
Event ID
63234
Address
1400 Parker St
Code information
Del Monte, 32 oz., best by 9/26/12, 9/27/12 and 9/28/12; 16 oz., best by 9/26/12 and 9/27/12; 8 oz., best by 9/26/12; chunks 7 oz., Lot 05262101 7 Eleven chunks, 6 oz., best by 9/28/12 and 9/29/12
Postal code
75215-2135
Report date
Jul 17, 2013
Product type
Food
Recall number
F-1610-2013
Classification
Class I
Recalling firm
Del Monte Fresh Produce North America, Inc
Product quantity
3071 unit total
Termination date
Jul 31, 2013
Reason for recall
In cooperation with the FDA's warning to not consume mangoes from Agricola Daniella in Mexico, Del Monte Fresh Produce N.A., Inc, is initiating a voluntary recall of 1,600 bowls of fresh-cut mangoes distributed to retail outlets due to the potential risk that the mangoes may contain Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frai
Voluntary / mandated
Voluntary: Firm initiated
Product description
Mango (Fresh Cut): Del Monte brand slices, 32 oz., UPC 7-62357-07532-1, 32 oz., UPC 7-17524 72503-5; 16 oz., UPC 7-17524-71902-7, 8 oz., UPC 7-17524-72506-7, UPC 7-17524-72506-6; Del Monte brand chunks, 7 oz., 7 Eleven brand chunks, 6 oz., UPC 0-52548-52070-0
Distribution pattern
Product was distributed directly to the states of Florida, Georgia, Missouri, North Carolina, Ohio, and Texas. Product was then shipped further from the firm's direct accounts.
Recall initiation date
Sep 20, 2012
Initial firm notification
Press Release
Center classification date
Jul 5, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1610-2013, published Jul 17, 2013. View the source record (openFDA) · FDA enforcement reports

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

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