Food Recall Check
Class I · High risk Terminated Initiated Mar 4, 2016 (11 years ago)

Eatin' Alive VEGAN GLUTEN FREE RAW thai peanut noodles recall

Recalled by Paige Common · Portland, OR, United States

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

Why it was recalled

Paige Common dba Eatin' Alive is recalling Thai Peanut Noodles and Thai Wrap due to undeclared allergen soy. The soy is a sub ingredient of tamari.

Undeclared allergens: Peanut Soy

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

Eatin' Alive VEGAN GLUTEN FREE RAW thai peanut noodles. Keep Refrigerated. 8oz UPC 0 91037 56624 9

Quantity: 24 units

Food: 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.

SELL BY: 3/8

Where it was sold

Oregon

FDA's distribution note: Oregon retail stores 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, soy; 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
Paige Common
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 4, 2016
In FDA report of
Aug 31, 2016
Terminated
Aug 23, 2016
FDA recall number
F-1971-2016 · event 73483
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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

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