FDA recall record

RMH Foods Gordon Choice Deli Style Tuna Salad, Refrigerated, 4 Lb recall — FDA F-0878-2021

Undeclared wheat and tuna

Class IIclassification
F-0878-2021official record ID
Sep 1, 2021report date

Recall record at a glance

Official recordF-0878-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRMH Foods
Report dateSep 1, 2021
Recall initiation dateAug 11, 2021
Quantity583 cases
LocationMorton, IL, United States

Official product description

Gordon Choice Deli Style Tuna Salad, Refrigerated, 4 Lb. retail unit, 2 4 Lb. retail units per wholesale case. Wholesale case labeled as Deli Style Tuna Salad The recalled product contains tuna salad, but it has two labels. The bottom container states Deli Style Chicken Salad, while the top lid label states Deli Style Tuna Salad. The Gordon Choice Deli Style Tuna Salad, UPC found on the lid is 0 9390113900 9. The Gordon Choice Deli Style Chicken Salad, UPC found on the bottom tub is 0 9390113903 0. If you purchased this product from GFS as an entire case, you are looking for: Cases of GFS item 139007, SALAD TUNA DELI 2-4# GCHC If you purchased this product from a GFS Store as an individual tub, you are looking for: Tubs of GFS item 139030, SALAD CHICKEN DELI 2-4# GCHC

Why the product was recalled

Undeclared wheat and tuna

Distribution information

Gordon Food Service retail stores and food service establishments in AL,FL, GA, IL, IN, KY, MI, MO, OH, PA, TN, VA, WV

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.