Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 20, 2019 (7 years ago)

All colors and sizes of Confectionery Arts International recall

Recalled by Confectionery Arts International, LLC · New Britain, CT, United States

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

Why it was recalled

Borosilicate glass material found in FDA Sample.

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

All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and sold prior to 4/25/19; 4g packed in 1/4 oz. jars and 14g packed in 1 oz. jars.

Quantity: 42,238 pcs

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.

All item codes manufactured and sold prior to 4/25/19.

Where it was sold

Arizona California Colorado Connecticut Florida Georgia Illinois Indiana Kentucky Maryland Maine Michigan Minnesota Missouri North Carolina New Jersey Nevada New York Ohio Oregon Pennsylvania Tennessee Texas Virginia Washington Wisconsin

FDA's distribution note: Distributed in 26 states: NC, IN, KY, FL, NY, OH, IL, AZ, MN, OR, PA, VA, CA, MI, TN, GA, MO, TX, WI, MD, NV, CT, CA, NJ, CO, WA, ME

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
Confectionery Arts International, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 20, 2019
In FDA report of
Sep 4, 2019
Terminated
Aug 31, 2020
FDA recall number
F-2089-2019 · event 83588
Official record
FDA enforcement report search