Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 11, 2018 (9 years ago)

Gourmet Cream Cheese Cinnamon Rolls recall

Recalled by Schwartz Brothers Restaurants dba Schwartz Brothers Bakery · Seattle, WA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Gourmet Cream Cheese Cinnamon Roll is recalled due to undeclared egg.

Undeclared allergen: Egg

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 Cream Cheese Cinnamon Rolls, packaged in a 16 oz. plastic clam shell container and sold under the Schwartz Brothers Bakery brand. The product UPC is 7 17887 65082 1. The product is read in parts: "***GOURMET CREAM CHEESE CINNAMON ROLLS***NET WT. 16 OZ***Produced By Schwartz Brothers Bakery Seattle, WA 98108***Contains Milk, Wheat, Soy. May Contain Egg, Peanuts, Tree Nuts***".

Quantity: 106 units

Food: Cheese Seafood & fish Spices & seasonings

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.

sell by date 03/15/18.

Where it was sold

Washington

FDA's distribution note: distributed in WA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to egg; 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
Schwartz Brothers Restaurants dba Schwartz Brothers Bakery
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 11, 2018
In FDA report of
Apr 4, 2018
Terminated
Apr 12, 2018
FDA recall number
F-0984-2018 · event 79497
Official record
FDA enforcement report search

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