FDA recall record

House of Spices (India) 1) Crispy Pistachio Cookies is labeled in part recall — FDA F-1390-2012

House of Spices (India) Inc., Orlando, FL is recalling 7 oz packages of Crispy Coconut Cookies, Crispy Almond Cookies, 7oz and 14 oz Crispy Pistachio…

Class Iclassification
F-1390-2012official record ID
Jun 20, 2012report date

Recall record at a glance

Official recordF-1390-2012
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHouse of Spices (India) Inc.
Report dateJun 20, 2012
Recall initiation dateApr 5, 2012
Quantity1) 13 cases; 2) 2 cases
LocationORLANDO, FL, United States

Official product description

1) Crispy Pistachio Cookies is labeled in part: "***VEGETARIAN***NO EGG***CRISPY***By TWI Foods***PISTACHIO COOKIES***Just Baked!***Biscuit Pistache***Net Wt./Poids Net 200g/7oz***TWI FOODS INC***1869 Cage Court, Mississauga, ON Canada L5S 1S3. 1-866-9-CRISPY*** ; 2) Crispy Pistachio Cookies is labeled in part: "***VEGETARIAN***NO EGG***CRISPY***By TWI Foods***PISTACHIO COOKIES***Just Baked!***Biscuit Pistache***Net Wt./Poids Net 400g/14oz***www.CrispyJustBaked.com***Ingredients: Wheat flour, soybean oil margarine, sugar, pista, cornstarch, (vegetable based soy lecithin and soy protein), corn syrup, baking powder, artificial flavor, salt, and ammonium carbonate.***6 27265 00161 2***"

Why the product was recalled

House of Spices (India) Inc., Orlando, FL is recalling 7 oz packages of Crispy Coconut Cookies, Crispy Almond Cookies, 7oz and 14 oz Crispy Pistachio Cookies manufactured by TWI Foods Inc. Ontario Canada. The products may contain undeclared milk and almonds.

Distribution information

Distributed to ethnic retail stores in Florida.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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