FDA recall record

Sage Creek Canned Peach Slices in Light Syrup or canned Peach Slices in recall — FDA F-1312-2013

potentially under processed and reports of swollen and bursting cans as well as discoloring fruit soon after opening the can and the fruit is undercooked…

Class IIclassification
F-1312-2013official record ID
Apr 17, 2013report date

Recall record at a glance

Official recordF-1312-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSage Creek Inc.
Report dateApr 17, 2013
Recall initiation dateFeb 8, 2013
Quantityfirm unwilling/unable to provide
LocationThe Dalles, OR, United States

Official product description

Canned Peach Slices in Light Syrup or canned Peach Slices in Heavy Syrup or canned Peach halves in Heavy Syrup. The PDP reads "HOOD-CREST ELBERTA PEACHES YELLOW FREESTONE SLICES IN LIGHT SYRUP NET WT. 28 OZ. (1LB. 12 OZ.) 793G" The back panel reads in part "***INGREDIENTS: PEACHES, WATER, SUGAR. MUIRHEAD CANNING CO. The Dalles, Ore. 97058***" The UPC on the label reads 7 88637 01111 7. The PDP reads "HOOD-CREST ELBERTA PEACHES YELLOW FREESTONE SLICES IN HEAVY SYRUP NET WT. 28 OZ. (1 LB. 12 OZ.) 793G" The back panel reads in part "***INGREDIENTS: PEACHES, WATER, SUGAR. Packed by MUIRHEAD CANNING CO. The Dalles, Ore. 97058. There is no UPC on the label. The PDP reads "HOOD-CREST ELBERTA PEACHES YELLOW FREESTONE HALVES IN HEAVY SYRUP NET WT. 28 OZ. (1LB. 12 OZ.) 793G" The back panel reads in part "*** INGREDIENTS: PEACHES, WATER, SUGAR MUIRHEAD CANNING CO. The Dalles, Ore. 97058***" There is no UPC on the label.

Why the product was recalled

potentially under processed and reports of swollen and bursting cans as well as discoloring fruit soon after opening the can and the fruit is undercooked (too firm), from consumers.

Distribution information

Western US

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: Telephone.

What to do next

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