FDA recall record

Torn Ranch Fruit Truffles - Cherry, Coconut, Key Lime, Lemon, Mango recall — FDA F-0173-2014

FDA inspection at the firm found that Yellow # 5 and 6 used in decoration on top of fruit truffles was not declared in the ingredient statement.

Class IIclassification
F-0173-2014official record ID
Nov 20, 2013report date

Recall record at a glance

Official recordF-0173-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTorn Ranch Inc.
Report dateNov 20, 2013
Recall initiation dateOct 25, 2013
Quantity3840 individual truffles
LocationPetaluma, CA, United States

Official product description

Fruit Truffles - Cherry, Coconut, Key Lime, Lemon, Mango, Pear, Pineapple and Tangelo flavors. (6 piece count/4.5 oz) Pear, Lemon, Key Lime, Coconut flavors contain FD&C Y5 and/or Y6; (9 piece count/7 oz) Pear, Cherry, Tangelo, Coconut, Lemon, Key Lime flavors contain FD&C Y5 and/or Y6 ; (12 piece count/9 oz) Mango, Pineapple, Tangelo, Cherry, Pear, Coconut, Key Lime, Lemon flavors contain FD&C Y5 and/or Y6; Firm also sells 2 piece count/1.5 oz products. However, this product only contains 2 strawberry flavors and do not contain FD&C Y5 and/or Y6. Sold to the hospitality industry. Product of the USA. Manufactured by Torn Ranch, Petaluma, CA 94954

Why the product was recalled

FDA inspection at the firm found that Yellow # 5 and 6 used in decoration on top of fruit truffles was not declared in the ingredient statement.

Distribution information

US only - CA, TX, FL, MS, WA, NC, MA, IN, NC, NY, PA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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.

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