The Traveler's Best Ham & Swiss on Pretzel Roll Smoked Ham and Swiss Cheese W...
FDA Recall #F-0895-2023 — Class II — April 24, 2023
Recall Summary
| Recall Number | F-0895-2023 |
| Date Initiated | April 24, 2023 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | GH Foods LLC |
| Location | Riverside, CA |
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
Reason for Recall
Undeclared allergen; sesame seeds
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution Pattern
U.S. distribution to the following: CA, CO, AZ, UT No foreign distribution.
Product Quantity
1805
Product Codes / Lot Numbers
Lot GHSC 002-GHSC 112 Expiration dates: 1/9/2023-4/26/2023 Lot GHCA 004-GHCA112 Expiration dates: 1/11/2023-4/26/2023
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.