Food Recall Check
Class I · High risk Terminated Initiated May 23, 2022 (4 years ago)

Taharka Brothers Peanut Butter Cup Ice Cream recall

Recalled by Taharka Brother's Ice Cream · Baltimore, MD, United States

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

Why it was recalled

May 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

Taharka Brothers Peanut Butter Cup Ice Cream 16 oz Pint Container: Paper cup with peanut butter cups along the bottom with a white background. Barcode: 38455-78827 2.5 Gallon: Brown and rectangular cardboard container with a white sticker label

Quantity: 16oz Pints: 1700 units 2.5gal Tubs: 59units

Food: Ice cream 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.

Expiration dates between 2023/03 and 2023/05.

Where it was sold

Maryland Virginia Washington

FDA's distribution note: Distributed in Taharka Brothers retail location as well as grocery stores in Maryland, Virginia, and Washington D.C.

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
Taharka Brother's Ice Cream
Initiated by
Voluntary: Firm initiated
Recall initiated
May 23, 2022
In FDA report of
Jun 15, 2022
Terminated
Sep 12, 2024
FDA recall number
F-1283-2022 · event 90346
Official record
FDA enforcement report search

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