Food Recall Check
Class I · High risk Terminated Initiated Jan 15, 2015 (12 years ago)

Garden Lites Kale & Quinoa Souffle recall

Recalled by classic cooking llc · Jamaica, NY, United States

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

Why it was recalled

Cumin contains undeclared peanut protein

Undeclared allergen: Peanut

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

Garden Lites Kale & Quinoa Souffle, NET WT 7 oz, UPC 7-04863-01730-3

Quantity: 192 units

Food: Leafy greens & salads Pasta, rice & grains

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.

1) LOT # 3219- EXP DATE 5/25/2016, 2) LOT # 33014-EXP DATE 5/26/2016, 3) LOT # 3517- EXP DATE 6/23/2016

Where it was sold

Nationwide.

FDA's distribution note: nationwide in retail stores

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; 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
classic cooking llc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 15, 2015
In FDA report of
Apr 15, 2015
Terminated
Jun 12, 2018
FDA recall number
F-1927-2015 · event 70285
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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