Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 17, 2022 (4 years ago)

Phil's Power Pancakes recall

Recalled by Phil's Power Pancake · Costa Mesa, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product found to contain wheat that is not declared on the label.

Undeclared allergen: Wheat

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

Phil's Power Pancakes 5 oz. individually wrapped units 5 varieties, including (Chocolate Hempseed, Cranberry, Raspberry, Mango, and Date) UPC: 8 3765448372 5

Quantity: 500 units per week

Food: Chocolate & candy Berries Fresh fruit

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.

No manufacturing codes

Where it was sold

California

FDA's distribution note: Product is distributed in the Los Angeles and Orange County area, exclusively within the state of California. Mr. Perota stated that the firm has used the recalled product label since the mid 1990's. Shelf life is approximately one week, however product could have been frozen.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; 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
Phil's Power Pancake
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 17, 2022
In FDA report of
Jan 4, 2023
Terminated
Jan 30, 2023
FDA recall number
F-0211-2023 · event 91181
Official record
FDA enforcement report search

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