Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 24, 2018 (8 years ago)

Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar recall

Recalled by Power Selles Imports dba Culinary Collective · Lynnwood, WA, United States

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

Why it was recalled

Matiz Apricot Bar Demi-luna 8.8 ounces bar is recalled because customer found two small plastic pieces in the product.

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

Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar, packaged in shrink wrap plastic, UPC 8 32924 00543 0. Product is labeled in parts: "***matiz RAW APRICOT ***100% Natural Ingredients: 92% dried apricots and almonds ****PRODUCED BY: Bio Vera, Losar de la Vera, C¿ceres***product of Spain*** Imported by Matiz Espa¿a, Lynnwood, WA 98087***".

Quantity: 78 cases (12 units per case)

Food: Salads, sandwiches & prepared foods

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.

Lot/batch #/39617, best before date 1/30/2019

Where it was sold

Colorado Florida Illinois New Hampshire New York Virginia

FDA's distribution note: distributed in CO, FL, IL, NH, NY, and VA.

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
Power Selles Imports dba Culinary Collective
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 24, 2018
In FDA report of
Aug 15, 2018
Terminated
Sep 6, 2018
FDA recall number
F-1754-2018 · event 80623
Official record
FDA enforcement report search

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