FDA recall record

Kettle Foods Krinkle Cut Cheddar and Sour Cream recall — FDA F-1788-2012

Metal fragments in raw material (lactic acid) of flavorings, recalled by manufacturing firm, were used in the product.

Class IIclassification
F-1788-2012official record ID
Aug 1, 2012report date

Recall record at a glance

Official recordF-1788-2012
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKettle Foods, Inc.
Report dateAug 1, 2012
Recall initiation dateJun 7, 2012
Quantity2462 cs+ 36 cs + 106 cs + 759 cs and 960 bags + 3515 cs + 360 cs + 20 bags = 7184 cs 980 bags
LocationSalem, OR, United States

Official product description

Kettle Brand Potato Chips, Krinkle Cut Cheddar and Sour Cream; 1) 6/2 oz (caddy) item # 0711770000, UPC 0 8114 11715 1; 2) 24/2 oz item # 0711714000, UPC 0 84114 11715 1; 3) 15/5 oz item # 0711718000, UPC 0 84114 11719 9; 4) 12/8.5 oz item #'s 0711726001 and 0711726500 (different numbers for different geographical locations of distribution), UPC 0 84114 11728 1; 5) 10/13 oz item # 0711716001, UPC 0 84114 11717 5; 6) 12/220 g item # 0711915000, UPC 0 84114 1190 5; 7) 10/397g item # 0711729000, UPC 0 84114 11731 1.

Why the product was recalled

Metal fragments in raw material (lactic acid) of flavorings, recalled by manufacturing firm, were used in the product.

Distribution information

36 customers Worldwide

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: 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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