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HILLSHIRE FARM
Recall · Class I2012-11-10Terminated

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

Some of the Jimmy Dean French Toast & Sausage Sandwiches were mislabeled on the back label with an ingredients statement for another product, resulting in undeclared allergens, egg and soy, not listed on the label.

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 HILLSHIRE FARM.

What the notice covered

Jimmy Dean French Toast & Sausage Sandwich, Net Wt 3.9 oz (110g); a food service individually butcher paper wrapped, fully cooked frozen sandwich; 12 sandwiches per 2.74 lb case; UPC 54500 51434

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-0724-2013
Kind of action
Recall
Dated
2012-11-10
Terminated
2016-04-11
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-0724-2013"

To see it in the FDA’s own words, search the reference number F-0724-2013 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