Food Recall Check
Class I · High risk Terminated Initiated Mar 6, 2020 (7 years ago)

HEB Tuscan Herb Chopped Salad Kit recall

Recalled by Dole Fresh Vegetables Inc · Monterey, CA, United States

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

Why it was recalled

Private brand customer received 3 complaints of consumers finding the incorrect master pack (kit with dressing and other toppings) in 12.6 oz. Tuscan Herb Chopped Kit. The dressing included was Sweet Thai which contains peanuts, tree nuts and wheat that were not declared on label.

Undeclared allergens: Peanut Tree nuts Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

HEB Tuscan Herb Chopped Salad Kit, 12.6 oz. UPC: 0-41220-40989-1

Quantity: 300 cases

Food: Leafy greens & salads

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.

Best by March 11, 2020; B055014 and B055015

Where it was sold

Texas

FDA's distribution note: TX only

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. The risk from an undeclared allergen is to people allergic to peanut, tree nuts, wheat; for anyone else the product is generally not a safety concern. 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
Dole Fresh Vegetables Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 6, 2020
In FDA report of
Mar 25, 2020
Terminated
Apr 13, 2020
FDA recall number
F-0840-2020 · event 85163
Official record
FDA enforcement report search

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