Lemon Dessert Bars packaged under Schwartz Brothers Bakery brand in a
Reason Lemon Dessert Bars product is recalled due to undeclared egg.
Everything Bagels" product is packed in a clear 4-pack plastic bag 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
Mislabeling. Product inside a plastic bag actually contains milk but mis-labeled as "Everything Bagels" and this label does not declare milk.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
"Everything Bagels" product is packed in a clear 4-pack plastic bag, with visible image of cheese melted on top of the bagels. This product has the UPC number 7 17887 23121 1. The product is labeled in parts: "***Everything Bagels***Net Wt. 16 oz (1 lb) 454 g***Produced By Schwartz Brothers Bakery Seattle, Renton WA***7 17887 23121 1***Schwartzbros.com***.
Quantity: 321 bags
Food: Bread & bakery
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.
Best By dates of 10/14/14 to 11/10/14
Where it was sold
Oregon Washington
FDA's distribution note: distributed in Oregon and Washington
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. 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
- Nov 6, 2014
- In FDA report of
- Dec 17, 2014
- Terminated
- Dec 10, 2014
- FDA recall number
- F-0704-2015 · event 69706
- Official record
- FDA enforcement report search
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