Food Recall Check
Class I · High risk Terminated Initiated Mar 7, 2023 (4 years ago)

Clio Strawberry Granola & Yogurt Parfait Bar recall

Recalled by Clio LLC · Piscataway, NJ, United States

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

Why it was recalled

Possible contamination 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

Clio Strawberry Granola & Yogurt Parfait Bar Net Wt. 1.94 OZ (55g ) UPC: 854021008152 Packaged in a cardboard box.

Quantity: 581 cases of 10 single units

Food: Milk & dairy Berries Pasta, rice & grains

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.

048C2023 Expiration date:4/30/2023

Where it was sold

California Florida Georgia Iowa Illinois Maine Minnesota Missouri North Carolina South Carolina Virginia Washington Wisconsin

FDA's distribution note: Product distributed to distribution centers in IL, SC, MO, WA, GA, MN, FL, NC, ME, and CA. Then further distributed to retail stores in IA, IL, VA, WI, and NC.

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
Clio LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 7, 2023
In FDA report of
Apr 12, 2023
Terminated
Sep 17, 2024
FDA recall number
F-0697-2023 · event 91865
Official record
FDA enforcement report search

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