Recall record at a glance
| Official record | F-2155-2012 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Ron Stockman Whole Foods |
| Report date | Sep 19, 2012 |
| Recall initiation date | Jul 27, 2012 |
| Quantity | UNKNOWN |
| Location | Ft Lauderdale, FL, United States |
Official product description
The Thousand Island Chicken Salad Roll is sold at the chef's case, self serve counter, or packaged. Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***1000 ISLAND CHICKEN SALAD ROLL 2 FOR 5***BREAD ( UNBLEACHED UNBROMATED WHEAT OR WHOLE WHEAT FLOUR, WATER, FLORIDA CRYSTALS SUGAR, PALM OIL, EGGS, NON FAT DRY MILK, ASCORBIC ACID, SALT, YEAST, CULTURED WHEAT FLOUR, SOY LECITHIN & NATURAL ENZYMES), CHICKEN ( CHICKEN, WATER, RICE STARCH, SALT), OR TURKEY, CAGE-FREE EGGS (EGGS, WATER, CITRIC ACID), CANOLA OIL, EGGS, FILTERED WATER, HONEY, VINEGAR, SEA SALT, DRY MUSTARD, LEMON JUICE, CUCUMBERS, CRYSTALIZED CANE JUICE, WATER, DISTILLED VINEGAR, SALT, DEHYDRATED PEPPERS, CALCIUM CHLORIDE, XANTHAN GUM, NATURAL SPICE FLAVORS, GUM ARABIC, CALCIUM CHLORIDE, DEHYDRATED BELL PEPPERS, SPICES (CELERY SEED), NATURAL FLAVORS ( CASSIA, CLOVE), CITRIC ACID, ONION, AGED CAYENNE RED PEPPERS, GARLIC POWDER, LIQUID AMINOS ( FORMULATED SOY PROTEIN, WATER), PAPRIKA, KETCHUP ( TOMATO PUREE, EVAPORATED CANE JUICE, SUGAR, WHITE VINEGAR, SALT, ONION POWDER & SPICES), CAPERS ( CAPERS, VINEGAR SALT), GARLIC, EXTRA VIRGIN OLIVE OIL, DILL, CABBAGE, CARROTS, SUGAR, CHILI, SALT, GUAR GUM, CITRIC ACID), AGED CAYENNE RED PEPPERS, PAPRIKA CONTAINS: WHEAT, EGGS, MILK, SOY.***"
Why the product was recalled
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.
Distribution information
Products were sold directly to the consumers though our Whole Foods Market Retail stores in the state of Florida.
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: Other.
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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