Food Recall Check
Class I · High risk Terminated Initiated Jun 14, 2014 (12 years ago)

Wegmans Cinnamon Raisin Buns recall

Recalled by Wegmans Food Markets, Inc. · Rochester, NY, United States

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

Why it was recalled

The Raisin Cinnamon Buns contain undeclared eggs which may also be raw. This poses a potential health risk to consumers if the product is consumed.

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

Wegmans Cinnamon Raisin Buns, NET WT. 12 OZ (340g), UPC 77890 92218 ---Baked by Wegmans Food Markets Inc. - Rochester, NY 14603

Quantity: 1,315 units

Food: 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.

BEST IF USED BY 6/19 TU (stamped on top of package)

Where it was sold

Massachusetts Maryland New Jersey New York Pennsylvania Virginia

FDA's distribution note: New York, Pennsylvania, New Jersey, Massachusetts, Virginia, and Maryland

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
Wegmans Food Markets, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 14, 2014
In FDA report of
Jul 23, 2014
Terminated
Jul 17, 2014
FDA recall number
F-2190-2014 · event 68551
Official record
FDA enforcement report search

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