Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 21, 2017 (9 years ago)

Fit & Active Chocolatey Chip Protein Meal Bars recall

Recalled by Leclerc Foods USA · Montgomery, PA, United States

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

Why it was recalled

Firm received reports of flexible pieces of yellow plastic found in Fit & Active Chocolatey Chip Protein Meal Bars.

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

Fit & Active Chocolatey Chip Protein Meal Bars; UPC: 41498 18695; Lot Code: Q209MY; Expiration date: May 24, 2018

Quantity: 2701 cs, 7 boxes/cs, 6 bars/box

Food: Chocolate & candy Chips & snacks

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.

UPC: 41498 18695; Lot Code: Q209MY; Expiration date: May 24, 2018

Where it was sold

Connecticut District of Columbia Delaware Florida Georgia Massachusetts Maryland North Carolina New Hampshire New Jersey New York Ohio Oklahoma Pennsylvania Rhode Island South Carolina Tennessee Texas Virginia Vermont West Virginia

FDA's distribution note: Connecticut, Delaware, Florida, Georgia, Massachusetts, Maryland, District of Columbia (DC), New Jersey, New Hampshire, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Vermont, Virginia, West Virginia

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
Leclerc Foods USA
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 21, 2017
In FDA report of
Dec 13, 2017
Terminated
Jul 3, 2019
FDA recall number
F-0422-2018 · event 78630
Official record
FDA enforcement report search

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