FDA recall record

Giant Eagle GetGo GNG 7 Inch Turkey N Swiss Sell By recall — FDA F-2025-2015

GetGo from Giant Eagle Voluntarily Recalls Select Grab-and-Go Subs Due to Undeclared Egg Allergen

Class Iclassification
F-2025-2015official record ID
Apr 29, 2015report date

Recall record at a glance

Official recordF-2025-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmGiant Eagle, Inc.
Report dateApr 29, 2015
Recall initiation dateMar 31, 2015
Quantity2332 units
LocationPittsburgh, PA, United States

Official product description

GetGo GNG 7 Inch Turkey N Swiss Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Milk, Soy, Wheat; UPC: 65567 20399 GetGo from Giant Eagle Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238 Sandwich is wrapped in plastic.

Why the product was recalled

GetGo from Giant Eagle Voluntarily Recalls Select Grab-and-Go Subs Due to Undeclared Egg Allergen

Distribution information

MD OH PA WV

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: E-Mail.

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.

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