Turkey and Havarti Sandwich NET WT. 8.55oz (242g) Perishable, Keep Refrigerated Contains Milk, Soy, Wheat. May contain e
Summary
The FDA issued a Class II for Turkey and Havarti Sandwich NET WT. 8.55oz (242g) Perishable, Keep Refrigerated by GH Foods LLC. Reason: Undeclared allergen; sesame seeds.
Details
Source
Food Recall
External ID
F-0896-2023
Action Date
2023-05-31
Status
Terminated
Category
food
Product Description
Turkey and Havarti Sandwich NET WT. 8.55oz (242g) Perishable, Keep Refrigerated Contains Milk, Soy, Wheat. May contain egg. Distributed By: Renaissance Food Group, LLC 1730 Eastridge Ave. Riverside, CA 92507 www.rfgfoods.com UPC 26766 15584
Lot/Code Info: GHSC 109,110,111,112,113,114 Expiration dates: 04/24/2023-04/29/2023
Quantity Affected: 1596
Reason for Recall
Undeclared allergen; sesame seeds
Distribution
U.S. distribution to the following: CA, CO, AZ, UT No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-24
Company
Riverside, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
GH Foods LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GH Foods LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GH Foods LLC have FDA actions?
GH Foods LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0896-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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