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Power Selles Imports dba Culinary Collective Recall: Matiz Apricot Bar Demi-luna 8.8 ounces bar is recalled because customer found two small plastic pieces in the product.

United States

TerminatedClass II

Company
Power Selles Imports dba Culinary Collective
Product
Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar, packaged i…
Recall date
July 24, 2018
Terminated
September 6, 2018
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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***". Not published in this source record 78 cases (12 units per case) Lot/batch #/39617, best before date 1/30/2019

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1754-2018
Event ID
80623
Status
Terminated
Classification
Class II
Company
Power Selles Imports dba Culinary Collective
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***".
Quantity
78 cases (12 units per case)
Reason
Matiz Apricot Bar Demi-luna 8.8 ounces bar is recalled because customer found two small plastic pieces in the product.
Recall initiation date
July 24, 2018
Report date
August 15, 2018
Classification date
Not published in this source record
Termination date
September 6, 2018
Distribution pattern
distributed in CO, FL, IL, NH, NY, and VA.
UPC, lot, and code information
Lot/batch #/39617, best before date 1/30/2019
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Power Selles Imports dba Culinary Collective

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Colorado 1
Florida 1
Illinois 1
New Hampshire 1
New York 1
Virginia 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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