HIGH RISK
Terminated
F-2142-2012
New York City Corned Beef on Rye sold at the chef's case, or packaged. Packaged product is labeled as listed below: "WHOLE FOODS MARKET***FANCY REUBEN SANDWICH WITH PASTRAMI OR CORNED BEEF***PASTRAMI OR CORNED BEEF (BEEF, WATER, SEA SALT, SUGAR, BEET POWDER, GARLIC POWDER, SPICES, GARLIC, BAY LEAF, MUSTARD SEED, ALLSPICE) HONEY MUSTARD COLESLAW ( GREEN & RED CABBAGE, CARROTS), HONEY MUSTARD DRESSING ( DIJON MUSTARD (DISTILLED VINEGAR, WATER, MUSTARD SEED, SALT, WHITE WINE, CITRIC ACID, TARTARIC ACID, SPICES, TURMERIC), WHOLEGRAIN MUSTARD ( WATER, GRAIN VINEGAR, MUSTARD SEED, SALT, SPICES), LEMON JUICE, CANOLA MAYONNAISE ( CANOLA OIL, EGGS, HONEY, VINEGAR, SALT, SPICES, LEMON JUICE), HONEY), OR CLASSIC COLESLAW ( GREEN & RED CABBAGE, CARROTS, CANOLA MAYONNAISE, HORSERADISH ( HORSERADISH, WATER, VINEGAR, SALT, NATURAL FLAVORINGS), SUGAR, FENNEL, LEMON PEPPER, CELERY SEED, APPLE CIDER VINEGAR (APPLE CIDER VINEGAR, WATER), SWISS CHEESE ( PART SKIM MILK, CHEESE CULTURE, SALT, ENZYMES), BREAD CIABATTA (ENRICHED WHEAT FLOUR ( WHEAT FLOUR, MALTED BARLEY FLOUR, NIACIN, REDUCED IRON, THIAMIN MONONITRATE, RIBOFLAVIN, FOLIC ACID), WATER, CANOLA OIL, EXTRA VIRGIN OLIVE OIL, RYE SOURDOUGH FLAVOR, SALT, YEAST). CONTAINS: MILK, EGGS, SOY, WHEAT.***"
Recalled by Ron Stockman Whole Foods
Classification
Class I — Dangerous or defective products that predictably could cause serious health problems or death.
Reason for Recall
Whole Foods Market in Florida recalled certain fresh food items sold in the prepared foods department and one item in the seafood department as they could of been made using raw yellow onions processed by Gill Onions, LLC. Gill Onions, LLC initiated a recall on their product due to possible Listeria monocytogenes contamination.
Product Details
Product Quantity
UNKNOWN
Product Type
Food
Code Info
None
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Products were sold directly to the consumers though our Whole Foods Market Retail stores in the state of Florida.
Company Location
Ft Lauderdale, FL, 33308
Timeline
Report Date
09/19/2012
Recall Initiated
07/27/2012
Classification Date
09/07/2012
Termination Date
09/19/2012
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: July 14, 2026
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