FDA recall record

GH Foods The Traveler's Best Ham & Swiss on Pretzel Roll Smoked Ham and recall — FDA F-0895-2023

Undeclared allergen; sesame seeds

Class IIclassification
F-0895-2023official record ID
May 31, 2023report date

Recall record at a glance

Official recordF-0895-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGH Foods LLC
Report dateMay 31, 2023
Recall initiation dateApr 24, 2023
Quantity1805
LocationRiverside, CA, United States

Official product description

The Traveler's Best Ham & Swiss on Pretzel Roll Smoked Ham and Swiss Cheese With Lettuce and Dijon Mustard on a Pretzel Roll Ingredients: Pretzel Bun (Enriched Wheat Flour (Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamin Mononitrate, Riboflavin, Folic Acid), Water, Sugar, Palm Oil, Butter (Milk), Contains 2% or less of each of: Salt, Yeast, Cultured Wheat Flour, Vinegar, Dried Whey (Whey (Milk), Benzeyl Peroxide (Decolorant), Wheat Gluten, Sodium Steareyl Lactyiate, Monoglycerides, Calcium Sulfate, Wheat Starch, Whole Wheat Flour, Sodium Hydroxide), Ham and Water (32% of Weight is Deed Ingredients, Cured with Water, Dextroze, Salt, Corn Syrup, Potassium Lactate, Modified Potato Starch, Sodium Phosphates, Sodium Erytherbate, Sodium Nitrate, Sodium Diacetate), Swiss Cheese (Pasteurized Milk, Cheese Culture, Salt, Enzymes), Lettuce, Dijon Mustard (Distilled White Vinegar, Mustard Seed, Water, Salt, White Wine, Citric Acid, Tartaric Acid, Fruit Pectin, Sugar, Spices). Contains Milk, Soy, Wheat. May Contain Egg, Soy. Distributed By: Renaissance Food Group LLC Rancho Cordova, CA 95570 www.rfgfoods.com 1-898-4-HWYFUN UPC 26766 52105

Why the product was recalled

Undeclared allergen; sesame seeds

Distribution information

U.S. distribution to the following: CA, CO, AZ, UT 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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