Food Recall Check
Class I · High risk Terminated Initiated Oct 26, 2012 (14 years ago)

Peanut Butter Pave recall

Recalled by B.T. McElrath Chocolatier, Inc · Minneapolis, MN, United States

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

Why it was recalled

The product has the potential to be contaminated with Salmonella.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Peanut Butter Pave, UPC code 693868102117 & 69386905312, in the following sizes: 1) 5 Piece Peanut Butter Pave, 63 Grams per pack, 12 Packs per case. 2) 2 Piece Peanut Butter Pave, 26 Grams per pack, 10 Packs per case. 3) Bulk Peanut Butter Pave, 415 Grams per pack.

Quantity: 6500 pieces

Food: Peanut butter

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 #'s 12031, 12046, 12159, 12201

Where it was sold

Alaska California Florida Illinois Massachusetts Minnesota Washington

FDA's distribution note: MN, CA, FL, WA, IL, AK, MA.

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. 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
B.T. McElrath Chocolatier, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 26, 2012
In FDA report of
Nov 21, 2012
Terminated
Dec 31, 2012
FDA recall number
F-0689-2013 · event 63582
Official record
FDA enforcement report search

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