FDA recall record

Oregon Freeze Dry Kirkland Signature brand Real Sliced Fruit, Item # 527069 recall — FDA F-1739-2014

Oregon Freeze Dry, Inc. is recalling Kirkland Signature brand Real Sliced Fruit due to contamination of Salmonella.

Class Iclassification
F-1739-2014official record ID
Apr 9, 2014report date

Recall record at a glance

Official recordF-1739-2014
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmOregon Freeze Dry Inc.
Report dateApr 9, 2014
Recall initiation dateMar 8, 2014
Quantity59,780 cases (20 pouches per case)
LocationAlbany, OR, United States

Official product description

Kirkland Signature brand Real Sliced Fruit, Item # 527069. The UPC on the master cardboard case is 0 96619 52706 9. Each cardboard case consists of 20 plastic pouches (7.41 oz): 10 pouches of Fuji Apple Slices, 5 pouches of Strawberry Banana Slices, and 5 pouches of Fuji Apple Slices with Cinnamon. The UPC on Fuji Apple Slices pouch is 0 96619 27072 9; The UPC Strawberry Banana Slices pouch is 0 96619 27070 5; The UPC Fuji Apple Slices with Cinnamon pouch is 0 96619 27071 2; Product is distributed by: Costco Wholesale Corp., P.O.Box 34535, Seattle, WA 98124-1535, 1-800-774-2678, www.costco.com

Why the product was recalled

Oregon Freeze Dry, Inc. is recalling Kirkland Signature brand Real Sliced Fruit due to contamination of Salmonella.

Distribution information

Product was distributed to Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Pennsylvania, South Carolina, South Dakota, Tennessee, Utah, Vermont, Virginia, Wisconsin, and Puerto Rico.

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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