Sub Buns sold under the Gonnella brand and packaged with 8 buns to a
Reason Undeclared milk allergen (whey)
Gourmet Sandwich Rolls sold under the Jewel brand and packaged with 8 rolls to a recall
Recalled by Gonnella Baking Co. · Schaumburg, IL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared milk allergen (whey)
Undeclared allergen: Milk
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Gourmet Sandwich Rolls sold under the Jewel brand and packaged with 8 rolls to a 20 oz. plastic transparent bag.
Quantity: 4,520 bags
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC: 0 41280 11563 3; Product Code: 11563
Where it was sold
Illinois Indiana Wisconsin
FDA's distribution note: US: IL, IN, WI
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Gonnella Baking Co.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 19, 2015
- In FDA report of
- Mar 18, 2015
- Terminated
- Apr 12, 2016
- FDA recall number
- F-1403-2015 · event 70311
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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