Check the Batch
Class ITerminated in FDA datasetRecall initiated Jul 22, 2022

Artisan Glaze 629159. Item# 20658745 / 30629159.LM1

Recalling firm: Lyons Magnus, Inc

Why it was recalled

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

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: Jul 25, 2024.

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

ProductArtisan Glaze 629159. Item# 20658745 / 30629159.LM1 Ingredients: Water, vegetable protein (pea) and less than 2% of dextrose, maltodextrin, modified food starch. Net Wt. 33.5 lb (15.19KG) Distributed by Kerry Beloit, WI 53511
Package size33.5 lb

FDA code information

Lot Code 1902 / Best By Date 12/27/2022; Lot Code 2902 / Best By Date 12/28/2022; Lot Code 3902 / Best By Date 12/29/2022. Expanded 8-10-2022 Lot Code 0702 / Best By Date 12/06/2022 Lot Code 0902 / Best By Date 12/26/2022 Lot Code 1702 / Best By Date 12/07/2022 Lot Code 2502 / Best By Date 11/18/2022 Lot Code 3502 / Best By Date 11/19/2022 Lot Code 4502 / Best By Date 11/20/2022 Lot Code 4602 / Best By Date 11/30/2022 Lot Code 5602 / Best By Date 12/01/2022 Lot Code 6602 / Best By Date 12/02/2022 Lot Code 7602 / Best By Date 12/03/2022 Lot Code 9602 / Best By Date 12/05/2022 Lot Code 9802 / Best By Date 12/25/2022

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Full FDA record and distribution details

Original product description

Artisan Glaze 629159. Item# 20658745 / 30629159.LM1 Ingredients: Water, vegetable protein (pea) and less than 2% of dextrose, maltodextrin, modified food starch. Net Wt. 33.5 lb (15.19KG) Distributed by Kerry Beloit, WI 53511

Original FDA recall reason

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Recall details

Recall number
F-1637-2022
Event ID
90667
FDA status
Terminated
Initiated
Jul 22, 2022
Reported
Sep 7, 2022
Classified
Aug 30, 2022
Terminated
Jul 25, 2024
Quantity
53,818,025 total units
Location
Fresno, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Nationwide

FDA source record · F-1637-2022

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

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