Food Recall Check
Class I · High risk Terminated Initiated Jul 17, 2015 (11 years ago)

Taco de Camar¿n con Imitaci¿n de King Crab recall

Recalled by Fabrica Confecciones Soto, Inc. · Canovanas, PR, United States

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

Why it was recalled

Undeclared allergens. Egg whites

Undeclared allergen: Egg

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

Taco de Camar¿n con Imitaci¿n de King Crab (Shrimp with Imitation King Crab Taco). Label reads in part : " *** Soto Fabrica & Confecciones"*** Tacos de Camarones*** Mantenganse Congelado"*** Peso Neto 5 lbs(2.3 kg)*** Manufacturado por: Fabrica Confecciones Soto, Inc. calle Autonomia #81 Canovanas, PR 00729***"

Quantity: 28 boxes, 20 units each

Food: Seafood & fish

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.

none

Where it was sold

Puerto Rico

FDA's distribution note: Puerto Rico 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 egg; 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
Fabrica Confecciones Soto, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 17, 2015
In FDA report of
Dec 16, 2015
Terminated
Apr 19, 2017
FDA recall number
F-0343-2016 · event 71873
Official record
FDA enforcement report search

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