Recall record at a glance
| Official record | F-0829-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | DUTCH TREAT SALADS, Inc. |
| Report date | Dec 25, 2013 |
| Recall initiation date | Oct 30, 2013 |
| Quantity | 894.75 LBS |
| Location | Zeeland, MI, United States |
Official product description
LIPARI OLDTYME Mexicali Dip, Keep Refrigerated, outer box Net Wt. 1 0 lbs. Distributed by Lipari Foods, Warren, Ml 48089 Inner container: Mexicali Dip, Dutch Treat Salads, Zeeland MI Net Wt. 5 Lbs. Mexicali Dip, Dutch Treat Salads, Zeeland , MI Net Wt 14 oz. 396.9 g Ingredients: INGREDIENTS CULTURED SOUR CREAM (PASTURIZED HOMOGENIZED MILK, CREAM, MODIFIED FOOD STARCH, NONFAT DRIED MILK, SODIUM PHOSPHATE, GUAR GUM, SODIUM NITRATE, POTASSIUM SORBATE, CARRAGEENAN, lOCUST BEAN GUM, ACTIVE CULTURE), BLACK( BEAN SALSA (TOMATOES, BLACK BEANS, WATER, CORN, TOMATO PASTE, RED Bell PEPPER, JALAPENO PEPPER, VINEGAR, SEASONING, Salt, SUG AR, SPICES, DEHYDRATED GARLIC, CILANTRO CONCENT, XA NTHAN GUM, POTASSIUM SORBATE, SODIUM BENZOATE, DRIED CHIVES), CHEDDAR CHEESE, MAYONNAISE (VGETABLE OIL [SOYBEAN AND CANOlLA OILS], EGG YOLK, WATER CORN SYRUP, VINIEGAR. SALT. SPICES. CALCIUM DISODIUM E'DTA) S'EASONING MIX. CHILl POWDER. POTASSIUM SOHBATE CONTAINS: EGG. MILK, SOY
Why the product was recalled
Product has potential Listeria monocytogenes contamination.
Distribution information
Distributor and retail direct accounts in Michigan with further distribution in Michigan, Ohio, Pennsylvania, and Wisconsin
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: 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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