FDA recall record

FLOWERS FOODS Swiss Rolls***Brand Name**Swiss Rolls Chocolate recall — FDA F-1817-2018

Products are recalled due to the potential salmonella in a whey powder sub-ingredient.

Class IIclassification
F-1817-2018official record ID
Aug 15, 2018report date

Recall record at a glance

Official recordF-1817-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFLOWERS FOODS
Report dateAug 15, 2018
Recall initiation dateJul 18, 2018
Quantity11,012 Cases
LocationThomasville, GA, United States

Official product description

Swiss Rolls***Brand Name**Swiss Rolls Chocolate (Snack) Cakes, NET WT OZ (g) PKGS***TWIN PACKS***Nutrition Facts***Ingredients: SUGAR, WHEY (MILK), ENRICHED BLEACHED FLOUR***DISTRIBUTED BY***UPC Sold under the brand names... Mrs. Freshley's - NET WT 12 OZ (340g) 6-2 OZ (57g) PKGS***Distributed by Flowers Foods Specialty Group, LLC, 5087 South Royal Atlanta Dr., Tucker, GA 30084***(8ct) - UPC 072250 01190 7*** (12 ct ) UPC 072250 90323 3 FOOD LION - 6 - 2.2 OZ (61g) PKGA NET WT 13 OZ (369g)***DISTRIBUTED BY:FOOD LION, LLC SALISBURY, NC 28147***UPC 035826 09277 9 HILL COUNTRY FARE-6-2 oz (57g) Pkgs/Net Wt. 12 oz (340g)***DISTRIBUTED BY H-E-B, SAN ANTONIS, TX 78204/MADE IN USA***UPC 041220 29658 3 Baker's Treats - 6 - 2.2 OZ (61g) PACKS NET WT 13 OZ (369g)*** Distributed by ALDI Inc., Batavia, IL 60510***UPC 041498 18838 2 MARKET SQUARE BAKERY - NET WT 12 OZ (340g) 6-2 OZ (57g) Twin Packs***Distributed by: Olivette Products, L.L.C., Bridgeton, MO 63044*** UPC 0 87381 76055 6 Great Value - 6-2.2 OZ (61g) PKGS NET WT 13 OZ (369g)***DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716***UPC 0 78742 14755 0

Why the product was recalled

Products are recalled due to the potential salmonella in a whey powder sub-ingredient.

Distribution information

Product was distributed in the following states: Swiss rolls were distributed nationwide. Bread was distributed in AL, FL, GA, NC, and SC.

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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