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

CANTALOUPE, HONEYDEW: Festival Foods-Best Of The Season 46981 H. Brooks Fruit Mix CH Net Wt 5.5…

Recalling firm: Cut Fruit Express, Inc.

Why it was recalled

Cut Fruit Express, Inc processed cantaloupe that was later recalled by the supplier DFI Marketing due to a positive Salmonella sample.

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: Nov 7, 2012.

Check your package

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

ProductCANTALOUPE, HONEYDEW: Festival Foods-Best Of The Season 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. H.Brooks 46981 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. Distributed by H. Brooks & Co. Mpls. MN 55112.
Package size5.5 oz
UPC038232469814

FDA code information

Use-by 9/11 to 9/14

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

Full FDA record and distribution details

Original product description

CANTALOUPE, HONEYDEW: Festival Foods-Best Of The Season 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. H.Brooks 46981 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. Distributed by H. Brooks & Co. Mpls. MN 55112.

Extracted codes and context

TypeCode / valueContext
UPC038232469814 Season 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. H.Brooks 46981 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. Distribu
UPC038232469814ks 46981 46981 H. Brooks Fruit Mix CH Net Wt 5.5 oz (156g) 6 per case 384 UPC# 0 3823246981 4. Distributed by H. Brooks & Co. Mpls. MN 55112.

Original FDA recall reason

Cut Fruit Express, Inc processed cantaloupe that was later recalled by the supplier DFI Marketing due to a positive Salmonella sample.

Recall details

Recall number
F-0036-2013
Event ID
63210
FDA status
Terminated
Initiated
Sep 13, 2012
Reported
Oct 17, 2012
Classified
Oct 9, 2012
Terminated
Nov 7, 2012
Quantity
372 cases total.
Location
Inver Grove Heights, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

MI, MN, WI

FDA source record · F-0036-2013

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

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