Food Recall Check
Class II · Moderate risk Terminated Initiated May 29, 2020 (6 years ago)

Healthy Choice Pesto and Egg bowls labeled in the following ways recall

Recalled by ConAgra Foods, INc. · Chicago, IL, United States

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

Why it was recalled

Product contained an ingredient (farro) that potentially contain small stones.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Healthy Choice Pesto and Egg bowls labeled in the following ways: 1) (for the US market) Healthy Choice Power Bowls Morning Pesto & Egg White Scramble, Net Wt. 7.2 OZ (204 g); UPC 0-72655-00083-4 2) (for the Canadian market) Healthy Choice, Power Bowls, All-Day Breakfast, Pesto & Egg White Scramble, 204 g, UPC 0 72655 00201 2

Quantity: 8,780 cases

Food: Sauces, dips & dressings

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.

US ProductL Lot: 5009003120, Best If Used By OCT 27 2020 Canadian Product: Lot: 5009003120, Best Before 20 OC 327

Where it was sold

Alabama California Connecticut Florida Georgia Illinois Kentucky Massachusetts Maine Minnesota Missouri North Carolina Nebraska New York Ohio Pennsylvania South Carolina Virginia Wisconsin

FDA's distribution note: Distributed to customers in AL, CA, CT, FL, GA, IL, KY, MA, ME, MN, MO, NC, NE, NY, OH, PA, SC, VA, WI, and to Canada.

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. 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
ConAgra Foods, INc.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 29, 2020
In FDA report of
Jun 17, 2020
Terminated
Aug 27, 2020
FDA recall number
F-0982-2020 · event 85749
Official record
FDA enforcement report search

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