Food Recall Check
Class I · High risk Terminated Initiated Aug 7, 2017 (9 years ago)

Taylor Farms Creamy Homestyle Coleslaw Kit recall

Recalled by Taylor Farms Retail, Inc. · Salinas, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

One production lot of Creamy Homestyle Coleslaw kit was inadvertently packed with organic dressing packet which contains egg and milk. Only egg is declared on product labeling.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Taylor Farms Creamy Homestyle Coleslaw Kit, dressing included. Green Cabbage, Carrots, Red Cabbage and Creamy coleslaw dressing. Triple washed and ready to enjoy. Salad Net. WT. 11.5 oz. , Dressing NET WT. 3. FL. oz. UPC: 030223040637

Quantity: 293 cases (6 x 11.5 ox. bags per case)

Food: Sauces, dips & dressings

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

lot code: TFRS212A07C; Best if Used by: 08-16-2017.

Where it was sold

California Florida West Virginia

FDA's distribution note: CA, WV, FL. The five cases that were shipped to WV and FL were determined to still be intact prior to issuing press release.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Taylor Farms Retail, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 7, 2017
In FDA report of
Aug 30, 2017
Terminated
Aug 31, 2017
FDA recall number
F-3457-2017 · event 77906
Official record
FDA enforcement report search

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