Check the Batch
Class ITerminated in FDA datasetRecall initiated Sep 13, 2012

SYSCO Imperial 4835718 30/4.5 OZ FRUIT MIX CANT/PINE/REDGRAPES 130249 & 130250 BEST BY 9/15/12…

Recalling firm: G.O. Fresh

Why it was recalled

G.O. Fresh in Minnesota is voluntarily recalling specific cut items that contain cantaloupe, which has been recalled by DFI Marketing, Inc. due to potential Salmonella…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 14, 2013.

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Compare the exact product and package details with the label you have.

ProductSYSCO Imperial 4835718 30/4.5 OZ FRUIT MIX CANT/PINE/REDGRAPES 130249 & 130250 BEST BY 9/15/12 & 9/16/12. SYSCO Imperial 7068657 4/5# FRUIT MIX CANT/PINE/RED GRAPE 130250 BEST BY 9/16/12.
Package size4.5 OZ

FDA code information

BEST BY 9/15/12 & 9/16/12.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

SYSCO Imperial 4835718 30/4.5 OZ FRUIT MIX CANT/PINE/REDGRAPES 130249 & 130250 BEST BY 9/15/12 & 9/16/12. SYSCO Imperial 7068657 4/5# FRUIT MIX CANT/PINE/RED GRAPE 130250 BEST BY 9/16/12.

Extracted codes and context

TypeCode / valueContext
best by9/15/12BEST BY 9/15/12 & 9/16/12.
best by9/15/12perial 4835718 30/4.5 OZ FRUIT MIX CANT/PINE/REDGRAPES 130249 & 130250 BEST BY 9/15/12 & 9/16/12. SYSCO Imperial 7068657 4/5# FRUIT MIX CANT/PINE/RED GRAPE 130250 BEST BY 9/16/12.
best by9/16/122. SYSCO Imperial 7068657 4/5# FRUIT MIX CANT/PINE/RED GRAPE 130250 BEST BY 9/16/12.

Original FDA recall reason

G.O. Fresh in Minnesota is voluntarily recalling specific cut items that contain cantaloupe, which has been recalled by DFI Marketing, Inc. due to potential Salmonella contamination.

Recall details

Recall number
F-0090-2013
Event ID
63267
FDA status
Terminated
Initiated
Sep 13, 2012
Reported
Oct 17, 2012
Classified
Oct 11, 2012
Terminated
Feb 14, 2013
Quantity
721 TOTAL CASES FOR ALL PRODUCTS
Location
Minneapolis, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Minnesota, Iowa, North Dakota and Wisconsin

FDA source record · F-0090-2013

Data updated September 16, 2026. View official FDA data ↗

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