Artisan Glaze (Lyons Magnus) – bacterial risk (2022)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
Lot Code 1902 / Best By Date 12/27/2022, Lot Code 2902 / Best By Date 12/28/2022
Products Sold
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
Lyons Magnus, Inc is recalling Artisan Glaze 629159. Item# 20658745 / 30629159.LM1 Ingredients: Water, vegetable protein (pea) a due to Findings and potential for Cronobacter sakazakii and Clostridium botulinum.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026