FDA recall record

Kettle Foods New York Cheddar recall — FDA F-1787-2012

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

Class IIclassification
F-1787-2012official record ID
Aug 1, 2012report date

Recall record at a glance

Official recordF-1787-2012
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKettle Foods, Inc.
Report dateAug 1, 2012
Recall initiation dateJun 7, 2012
Quantity805 cs + 468 cs + 144 cs + 169 cs + 84 cs + 2800 bags + 960 bags = 1670 cs + 3760 bags
LocationSalem, OR, United States

Official product description

Kettle Brand Potato Chips, New York Cheddar; 1) 24/1.5oz, item # 0712278000, UPC 0 8114 11271 2; 2) 24/2 oz item # 0703320000 UPC 0 84114 03320 8; 3) 15/5 oz item # 0710863000, UPC 0 84114 0094 1; 4) 12/8.5 oz item #'s 0710813001 and 0710813500 (different numbers for different geographical locations of distribution), UPC 0 84114 10813 5; 5) Canadian item 12/220 g item # 0711920000, UPC 0 84114 11907 0; 6) 100/5 oz as part of a display, item # 0703450000; 7) Shipper containing 48/8.5 oz, item # 0711651001.

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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