FDA recall record

Dole Chopped Kit Teriyaki Pineapple iceberg lettuce green leaf recall — FDA F-0842-2023

Undeclared allergen, milk, due to incorrect masterpack.

Class IIclassification
F-0842-2023official record ID
May 3, 2023report date

Recall record at a glance

Official recordF-0842-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDole Fresh Vegetables Inc.
Report dateMay 3, 2023
Recall initiation dateApr 13, 2023
Quantity181 cases
LocationMonterey, CA, United States

Official product description

Dole Chopped Kit Teriyaki Pineapple iceberg lettuce green leaf lettuce red cabbage sliced almonds teriyaki pineapple dressing crunchy noodles dried pineapples carrots Salad & Topping Net Wt.: 7.5 oz (212 g) Dressing Net: 1.9 fl oz (57 mL) Total Net Wt: 98.8 oz (276 g) Thoroughly Washed Perishable/Keep Refrigerated Ingredients: vegetables: green leaf lettuce, iceberg lettuce, carrots, red cabbage. Dressing: water, sugar, soy sauce (water, wheat, soybean, and salt), pineapple juice concentrate, soybean oil, distilled vinegar, garlic juice, dehydrated garlic, molasses, sesame oil. Contains less than 2% of cilantro, salt, xanthan gum, sesame seed, spice, natural flavor. Dried pineapple: pineapple, cane sugar, citric acid. almonds. chow mein noodles: enriched wheat flour (flour, niacin, reduced iron, thiamine mononitrate (vitamin B1), riboflavin (vitamin B2), folic acid), non-GMO soybean oil, barley flour, water, salt. Contains: wheat, tree nuts (almonds), sesame, soy Distributed By Dole Fresh Vegetables, Inc. Monterey, CA 93940

Why the product was recalled

Undeclared allergen, milk, due to incorrect masterpack.

Distribution information

U.S. distribution to the following: FL, PA, VA, TN, LA No foreign distribution.

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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