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Giant Eagle
Recall · Class I2015-03-22Terminated

Contains egg without saying so on the label, which matters if you are allergic to it.

Little Italy Panini contains Undeclared Egg.

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming Giant Eagle.

What the notice covered

Packed in rigid plastic clam shell container: Giant Eagle Little Italy Panini Cold; Sell By: (all dates up to and including) 3/24/2015; PLU #97525; Net Wt 13oz; Contains Wheat, Milk, Fish (Anchovy); Keep Refrigerated ; Giant Eagle Little Italy Panini Hot; Sell By: (all dates up to and including) 3/22/2015; PLU: 7369; Net Wt 16oz; Contains Wheat, Milk, Fish (Anchovy).

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class I means

The FDA’s most serious class: a reasonable probability that using the product will cause serious health consequences or death.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-1931-2015
Kind of action
Recall
Dated
2015-03-22
Terminated
2015-07-27
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

We have not matched this notice to any product in our database — usually because it named no barcode we hold. Products may still have been affected.

How we are treating it

This notice concerns the product line itself or how it was produced.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-1931-2015"

To see it in the FDA’s own words, search the reference number F-1931-2015 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site