Food Recall Check
Class I · High risk Terminated Initiated Sep 12, 2013 (13 years ago)

Schwebel's Golden Rich Bun with Honey recall

Recalled by Schwebel Baking Company · Youngstown, OH, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared eggs.

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

Schwebel's Golden Rich Bun with Honey, 18 oz plastic bag, 12 count, UPC 0 71319 00083 8 Product labeled in part, "INGREDIENTS: ENRICHED WHEAT FLOUR***CONTAINS: WHEAT, SOY SCHWEBEL BAKING CO. YOUNGSTOWN, OH 44501"

Quantity: 12,642/18 oz/12 count plastic 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.

Lot #CAFC8W, Best By Sept 21, Lot #CAFC7B, Best By Sept 20

Where it was sold

Indiana Michigan New York Ohio Pennsylvania West Virginia

FDA's distribution note: The product was shipped to the following states: IN, MI, NY, OH, PA & WV.

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 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
Schwebel Baking Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 12, 2013
In FDA report of
Nov 6, 2013
Terminated
Apr 28, 2014
FDA recall number
F-0086-2014 · event 66265
Official record
FDA enforcement report search