FDA recall record

CORFU TASTY GYROS 4 tubs per case recall — FDA F-0430-2025

Potential for Salmonella

Class Iclassification
F-0430-2025official record ID
Feb 5, 2025report date

Recall record at a glance

Official recordF-0430-2025
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCORFU TASTY GYROS
Report dateFeb 5, 2025
Recall initiation dateDec 2, 2024
Quantity289 cases of 0.5 gallon tubs and 25 5 gallon pails
LocationBensenville, IL, United States

Official product description

Corfu Tzatziki sauce packaged in half gallon plastic tubs, 4 tubs per case. Mediterranean Tzatziki sauce packaged in half gallon plastic tubs, 4 tubs per case. Unbranded Tzatziki sauce packaged in half gallon plastic containers, 4 tubs per case. Corfu Tzatziki sauce packaged in 5 gallon plastic pails.

Why the product was recalled

Potential for Salmonella

Distribution information

IA, IL, IN, MI, MN, NY, TX, WI, Kuwait.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.