Class ITerminated in FDA datasetRecall initiated Nov 17, 2023

Bix Produce Mixed Fruit with Grapes products containing Cantaloupe, Honeydew, Pineapple, and…

Recalling firm: FreshPoint Bix Produce Company, LLC

Why it was recalled

Potential Salmonella contamination.

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: Jan 15, 2025.

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

ProductBix Produce Mixed Fruit with Grapes products containing Cantaloupe, Honeydew, Pineapple, and Red Grapes. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12210, Fruit, Chunk Mixed 1/2" w/Grps, 5 lb. 2. Item # 12215, Fruit, Chunk Mixed 1/2" w/Grape 20 lb. 3. Item # 12246, Fruit, Chunk Mxd 1" Melon w/Grp 20 lb. 4. Item # 12250, Fruit, Chunk Mixed w/Grape 5 lb. 5. Item # 12255, Fruit, Chunk Mixed 1" w/Grape 20 lb.
Package size5 lb

FDA code information

Lot number / Sales Order #: 1. P2760602-00. 2. P2759812-00, P2760610-00. 3. P2760548-00, P2765086-00, P2765880-00, P5202380-00, P5221569-00. 4. P2765100-00, P2765869-00. 5. P2765330-00, P2765548-00, P2765785-00, P2765896-00.

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Full FDA record and distribution details

Original product description

Bix Produce Mixed Fruit with Grapes products containing Cantaloupe, Honeydew, Pineapple, and Red Grapes. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12210, Fruit, Chunk Mixed 1/2" w/Grps, 5 lb. 2. Item # 12215, Fruit, Chunk Mixed 1/2" w/Grape 20 lb. 3. Item # 12246, Fruit, Chunk Mxd 1" Melon w/Grp 20 lb. 4. Item # 12250, Fruit, Chunk Mixed w/Grape 5 lb. 5. Item # 12255, Fruit, Chunk Mixed 1" w/Grape 20 lb.

Original FDA recall reason

Potential Salmonella contamination.

Recall details

Recall number
F-0669-2024
Event ID
93471
FDA status
Terminated
Initiated
Nov 17, 2023
Reported
Dec 13, 2023
Classified
Jan 2, 2024
Terminated
Jan 15, 2025
Quantity
215 units
Location
Little Canada, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

IA, MN, ND, WI

FDA source record · F-0669-2024

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

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