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Giant Eagle recalls MD Dip-Rueben PLU# 24659500000. Expiration date 8/6/2020. Ingredients: REUBEN DIP [COOKED CORNED BEEF ROUND (CURED WITH
Recalled September 9, 2020 · FDA recall F-1389-2020 · Giant Eagle
Hazard
Potential contamination with Salmonella Newport in onions and prepared foods containing onions. · FDA Class I
Units
Unknown
Sold at
Product was produced and sold in Giant Eagle and Market District locations in IN, OH, MD, WV and PA.
Description
Potential contamination with Salmonella Newport in onions and prepared foods containing onions.
Product
MD Dip-Rueben PLU# 24659500000. Expiration date 8/6/2020. Ingredients: REUBEN DIP [COOKED CORNED BEEF ROUND (CURED WITH UP TO 15% OF A SOLUTION OF: WATER, SALT, SUGAR, SODIUM PHOSPHATE, POTASSIUM LACTATE, SODIUM ERYTHORBATE, SODIUM NITRITE, SODIUM DIACETATE, GARLIC POWDER, EXTRACTIVES OF SPICES), CREAM CHEESE (PASTEURIZED MILK AND CREAM, CHEESE CULTURE, SALT, STABILIZERS [CAROB BEAN AND/OR XANTHAN AND/OR GUAR GUMS]), SOUR CREAM (CULTURED CREAM, ENZYMES), THOUSAND ISLAND DRESSING (SOYBEAN OIL, CHILI SAUCE [TOMATO PUREE (WATER, TOMATO PASTE), SUGAR, DISTILLED VINEGAR, SALT, NATURAL FLAVOR, SPICE, ONION POWDER, GARLIC POWDER], HIGH FRUCTOSE CORN SYRUP, WATER, DISTILLED VINEGAR, SWEET RELISH [CUCUMBERS, HIGH FRUCTOSE CORN SYRUP, DISTILLED VINEGAR, SUGAR, SALT, MUSTARD SEEDS, DICED RED PEPPERS, WATER, XANTHAN GUM, NATURAL FLAVOR], EGG YOLK, CONTAINS LESS THAN 2% OF SALT, MUSTARD FLOUR, XANTHAN GUM, POLYSORBATE 60, DRIED ONION, SODIUM BENZOATE [PRESERVATIVE], DRIED GARLIC, OLEORESIN PAPRIKA [COLOR], CALCIUM DISODIUM EDTA [TO PROTECT FLAVOR], DRIED RED BELL PEPPER), SAUERKRAUT (CABBAGE, WATER, SALT, PRESERVATIVES [SODIUM BENZOATE, SODIUM BISULFITE]), YELLOW ONION, RELISH (CUCUMBERS, WATER, VINEGAR, SALT, RED BELL PEPPER, CALCIUM CHLORIDE, ALUM, XANTHAN GUM, 0.1% SODIUM BENZOATE [PRESERVATIVE], NATURAL FLAVORS, POLYSORBATE 80, YELLOW 5), SALT, CARAWAY SEED, GROUND BLACK PEPPER].
Manufacturer(s)
Giant Eagle
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →