Check the Batch
Class IITerminated in FDA datasetRecall initiated Jul 24, 2018

Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar, packaged in shrink wrap plastic

Recalling firm: Power Selles Imports dba Culinary Collective

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.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 6, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductMatiz 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***".
Package size8.8 ounces
UPC832924005430

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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***".

Extracted codes and context

TypeCode / valueContext
UPC832924005430aw 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 ****

Original FDA recall reason

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

Recall details

Recall number
F-1754-2018
Event ID
80623
FDA status
Terminated
Initiated
Jul 24, 2018
Reported
Aug 15, 2018
Classified
Aug 3, 2018
Terminated
Sep 6, 2018
Quantity
78 cases (12 units per case)
Location
Lynnwood, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

distributed in CO, FL, IL, NH, NY, and VA.

FDA source record · F-1754-2018

Data updated September 16, 2026. View official FDA data ↗

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