FDA recall record

Triple B Broccoli Salad Kit, Produced by CP Fresh of Seattle, WA, 1 x 8 recall — FDA F-0157-2018

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

Class Iclassification
F-0157-2018official record ID
Nov 8, 2017report date

Recall record at a glance

Official recordF-0157-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTriple B Corporation
Report dateNov 8, 2017
Recall initiation dateOct 20, 2017
Quantity113 cases
LocationSeattle, WA, United States

Official 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).

Why the product 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 has been recalled by vendor Mann Packing of Salinas, California.

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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