Triple B Corporation Recall: Salad Kit, Super Slaw CPF 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.

🇺🇸 United States

1. October 20, 2017 - Recall initiated
2. November 8, 2017 - Reported by source
3. December 6, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0159-2018

Event ID

78335

Status

Terminated

Classification

Class I

Company

Triple B Corporation

Product description

Salad Kit, Super Slaw CPF, Produced by CP Fresh of Seattle, WA, 1 x 6 lb. per case, UPC 45009 87788 8 The ingredients are: Nappa Cabbage, Dressing (Canola Oil, Water, High Fructose Corn Syrup, Honey, Yellow Mustard [Vinegar, Water, Mustard Seed, Salt, Turmeric (color), Spice], Distilled Vinegar, Egg Yolk, Salt, Dired Onion, Xanthan Gum, Spice, Mustard Flour, Sodium Benzoate and Potassium Sorbate [Preservatives], Carrots, Turnips, Broccoli, Beets, Sunflower seeds (Sunflower Kernels, Salt, Sunflower Oil), Dried Cranberries (Cranberries, Sugar, Sunflower Oil).

Quantity

1 bag

Reason

Salad Kit, Super Slaw CPF 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 initiation date

October 20, 2017

Report date

November 8, 2017

Classification date

Not published in this source record

Termination date

December 6, 2017

Distribution pattern

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

UPC, lot, and code information

Use by Dates: 10/15/2017 to 10/21/2017

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 78335 with 10 other product entries in Public Health Trace.

Responsible company: Triple B Corporation

Other recalls from Triple B Corporation

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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