Food Recall Check
Class I · High risk Terminated Initiated Jun 14, 2017 (9 years ago)

Wildway Apple Cinnamon Grain-Free Granola recall

Recalled by Wildway LLC · San Antonio, TX, United States

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

Why it was recalled

Potential to be contaminated with Listeria monocytogenes.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

Wildway Apple Cinnamon Grain-Free Granola 8 oz and 10 oz UPC: 85866005190 and UPC: 864352000015 packaged in plastic bag

Quantity: 459 cases

Food: Fresh fruit Pasta, rice & grains 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.

lots: 096, 097

Where it was sold

Nationwide.

FDA's distribution note: Nationwide throughout the US.

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
Wildway LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 14, 2017
In FDA report of
Jul 19, 2017
Terminated
Aug 15, 2018
FDA recall number
F-2539-2017 · event 77552
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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