Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz. UPC 0 13454 38313 1. Each kit contains 6 Pitas, Gyro Meat,
Summary
The FDA issued a Class I for Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz. UPC 0 13454 38313 1. by Reser's Fine Foods, Inc.. Reason: Salmonella. Beef & Lamb Gyro Sandwich Express Meal Kit contains implicated cucumber in the tzatziki sauce 3oz. cup..
Details
Source
Food Recall
External ID
F-0362-2025
Action Date
2025-01-08
Status
Terminated
Category
food
Product Description
Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz. UPC 0 13454 38313 1. Each kit contains 6 Pitas, Gyro Meat, Tzatziki Sauce 3oz. cups, Fire Feta Sauce, Feta Cheese Crumbles. Packaged in clear plastic clamshell. Distributed by Fresh Creative Foods, Vista CA.
Lot/Code Info: Kit has use by dates: 12/24/2024 12/25/2024 12/28/2024 1/2/2025 1/6/2025
Quantity Affected: 5271 cases
Reason for Recall
Salmonella. Beef & Lamb Gyro Sandwich Express Meal Kit contains implicated cucumber in the tzatziki sauce 3oz. cup.
Distribution
Distributed in AZ, CA, CO, FL, GA, IL, IN, KS, LA, MD, MN, MO, NC, NY, OH, OK, TX, UT and WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-06
Company
Beaverton, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Reser's Fine Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Reser's Fine Foods, Inc. have FDA actions?
Reser's Fine Foods, Inc. has 62 FDA actions in our database, including 62 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0362-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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