Class ITerminated in FDA datasetRecall initiated Dec 6, 2024

Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz.

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

Salmonella. Beef & Lamb Gyro Sandwich Express Meal Kit contains implicated cucumber in the tzatziki sauce 3oz. cup.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 26, 2025.

Check your package

Compare the exact product and package details with the label you have.

ProductBeef & 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.
Package size31.8oz
UPC013454383131

FDA code information

Kit has use by dates: 12/24/2024 12/25/2024 12/28/2024 1/2/2025 1/6/2025

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original 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.

Extracted codes and context

TypeCode / valueContext
UPC013454383131Beef & 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

Original FDA recall reason

Salmonella. Beef & Lamb Gyro Sandwich Express Meal Kit contains implicated cucumber in the tzatziki sauce 3oz. cup.

Recall details

Recall number
F-0362-2025
Event ID
95937
FDA status
Terminated
Initiated
Dec 6, 2024
Reported
Jan 8, 2025
Classified
Dec 31, 2024
Terminated
Feb 26, 2025
Quantity
5271 cases
Location
Beaverton, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed in AZ, CA, CO, FL, GA, IL, IN, KS, LA, MD, MN, MO, NC, NY, OH, OK, TX, UT and WY.

FDA source record · F-0362-2025

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.