Class ITerminated in FDA datasetRecall initiated Oct 20, 2017

Broccoli Salad Kit, Produced by CP Fresh of Seattle, WA, 1 x 8 lb. per case

Why it was recalled

Down-stream from Mann Packing recall #78326. Broccoli Salad Kit is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item…

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: Dec 6, 2017.

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ProductBroccoli Salad Kit, Produced by CP Fresh of Seattle, WA, 1 x 8 lb. per case, UPC 45009 85362 2. The ingredients are: BROCCOLI, BROCCOLI SALW (BROCCOLI, CARROTS, RED CABBAGE), COLESLAW DRESSING (SOYBEAN OR CANOLA OIL, SUGAR, WATER, EGGS, CIDER VINEGAR, WHITE VINEGAR, LEMON JUICE CONCENTRATE, SALT, MUSTARD FLOUR, SPICES, XANTHAN GUM, POTASSIUM SORBATE AND SODIUM BENZOATE [AS PRESERVATIVES], CITRIC ACID, CALCIUM DISODIUM EDTA [TO PROTECT FLAVOR], ONIONS, RAISINS, SUNFLOWER SEEDS (SUNFLOWER SEEDS, SOYBEAN OIL, SALT).

Package size8 lb

FDA code information

Use by Dates: 10/14/2017 to 10/26/2017

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Full FDA record and distribution details

Original product description

Broccoli Salad Kit, Produced by CP Fresh of Seattle, WA, 1 x 8 lb. per case, UPC 45009 85362 2. The ingredients are: BROCCOLI, BROCCOLI SALW (BROCCOLI, CARROTS, RED CABBAGE), COLESLAW DRESSING (SOYBEAN OR CANOLA OIL, SUGAR, WATER, EGGS, CIDER VINEGAR, WHITE VINEGAR, LEMON JUICE CONCENTRATE, SALT, MUSTARD FLOUR, SPICES, XANTHAN GUM, POTASSIUM SORBATE AND SODIUM BENZOATE [AS PRESERVATIVES], CITRIC ACID, CALCIUM DISODIUM EDTA [TO PROTECT FLAVOR], ONIONS, RAISINS, SUNFLOWER SEEDS (SUNFLOWER SEEDS, SOYBEAN OIL, SALT).

Original FDA recall reason

Down-stream from Mann Packing recall #78326. Broccoli Salad Kit is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.

Recall details

Recall number: F-0157-2018
Event ID: 78335
FDA status: Terminated
Initiated: Oct 20, 2017
Reported: Nov 8, 2017
Classified: Nov 13, 2017
Terminated: Dec 6, 2017
Quantity: 113 cases
Location: Seattle, WA, 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

distributed in Alaska, Idaho, Montana, Oregon, and Washington

FDA source record · F-0157-2018

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

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