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Winn-Dixie Stores Inc.
Recall · Class II2012-08-16Terminated

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

Undeclared allergen, soy lecithin.

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 Winn-Dixie Stores Inc..

What the notice covered

Southern Home Cranberry Nut Antioxidant Blend, Trail Mix, Net Wt. 16oz. (1 LB) 454g, Distributed by Southern Home, P.O. Box 99, Mauldin, SC 29662.

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 II means

The FDA’s middle class: use of the product may cause temporary or medically reversible health consequences, and the probability of serious harm is remote.

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-1984-2012
Kind of action
Recall
Dated
2012-08-16
Terminated
2013-01-24
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

Nobody has yet assessed whether this notice concerns the products we track for this company, so it is not shown on product pages.

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-1984-2012"

To see it in the FDA’s own words, search the reference number F-1984-2012 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