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Reser's Fine Foods, Inc. Recall: Salmonella. Item 404885, Gyro Kit No Trays contains implicated cucumber in the tzatziki sauce cup.

United States

TerminatedClass I

Company
Reser's Fine Foods, Inc.
Product
FCF Item 404885, Gyro Kit No Trays. Each box consists of 2/5…
Recall date
December 6, 2024
Terminated
February 26, 2025
Source
FDA

Reason for recall

Salmonella. Item 404885, Gyro Kit No Trays contains implicated cucumber in the tzatziki sauce cup.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
FCF Item 404885, Gyro Kit No Trays. Each box consists of 2/5.25lbs. packages. UPC 0 13454 38158. Distributed by Fresh Creative Foods, Vista CA. Each kit consists of 8 bags of Traditional Pita Bread, 2/32oz. bags of Gyro Slices, 2 Sleeves of 4/2oz. cups premium Tzatziki sauce, 2 sleeves of 4/2oz. cups Fire Feta sauce, and label #5108 Gyro on Premise. This product is sold to consignees for further assemble/repack and each 5.25lbs. tray is not sold directly to consumers. Not published in this source record 30 cases Kit has Use By date of 1/2/2025. Batch B1842582

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0364-2025
Event ID
95937
Status
Terminated
Classification
Class I
Company
Reser's Fine Foods, Inc.
Product description
FCF Item 404885, Gyro Kit No Trays. Each box consists of 2/5.25lbs. packages. UPC 0 13454 38158. Distributed by Fresh Creative Foods, Vista CA. Each kit consists of 8 bags of Traditional Pita Bread, 2/32oz. bags of Gyro Slices, 2 Sleeves of 4/2oz. cups premium Tzatziki sauce, 2 sleeves of 4/2oz. cups Fire Feta sauce, and label #5108 Gyro on Premise. This product is sold to consignees for further assemble/repack and each 5.25lbs. tray is not sold directly to consumers.
Quantity
30 cases
Reason
Salmonella. Item 404885, Gyro Kit No Trays contains implicated cucumber in the tzatziki sauce cup.
Recall initiation date
December 6, 2024
Report date
January 8, 2025
Classification date
Not published in this source record
Termination date
February 26, 2025
Distribution pattern
Distributed in AZ, CA, CO, FL, GA, IL, IN, KS, LA, MD, MN, MO, NC, NY, OH, OK, TX, UT and WY.
UPC, lot, and code information
Kit has Use By date of 1/2/2025. Batch B1842582
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 95937 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Reser's Fine Foods, Inc.

Product
FCF Item 404884, Gyro Kit With Trays. Each tray consists of…
Published
January 8, 2025
Distribution
Distributed in AZ, CA, CO, FL, GA, IL, I…

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Product
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Published
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Distribution
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Responsible company: Reser's Fine Foods, Inc.

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Arizona 1
California 1
Colorado 1
Florida 1
Georgia 1
Illinois 1
Indiana 1
Kansas 1
Louisiana 1
Maryland 1
Minnesota 1
Missouri 1
North Carolina 1
New York 1
Ohio 1
Oklahoma 1
Texas 1
Utah 1
Wyoming 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.