Food Recall Check
Class I · High risk Terminated Initiated Oct 17, 2017 (9 years ago)

Weis, Sunbury PA; BLT Sandwich recall

Recalled by Weis Markets, Inc., Ice Cream Division · Sunbury, PA, United States

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

Why it was recalled

The firm is recalling their Store Made BLT sandwich due to undeclared egg found in the mayonnaise ingredient. The firm received an illness complaint reporting that egg was not declared in the mayonnaise ingredient.

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

Weis, Sunbury, PA; BLT Sandwich; 1 CT

Quantity: 452 units

Food: Salads, sandwiches & prepared foods

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: (from) 5/31/17 to 10/17/17; UPC: 2059278003006

Where it was sold

Delaware Maryland New Jersey New York Pennsylvania Virginia

FDA's distribution note: U.S.: PA,NJ,NY,MD,VA, DE

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
Weis Markets, Inc., Ice Cream Division
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 17, 2017
In FDA report of
Nov 1, 2017
Terminated
Oct 26, 2017
FDA recall number
F-0035-2018 · event 78310
Official record
FDA enforcement report search

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