Sysco Imperial Thickened Dairy Drink (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
Sysco Imperial Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Made with Grade A 2% Fat Milk, Vitamins A & D. Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 74865-94550 9. Reorder # 0429357. 24 count case UPC 10074865945506. 2. 32 FL OZ (1 QT) 946mL UPC 7 34730-55614 7. Reorder # 4254296. 12 count case UPC 10734730556144. Refrigerate prior to serving. Shake well. Distributed by Sysco Corporation, Houston, Tex
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
1. 8 oz. cartons Lot Code 4212 / Best By Date 11/30/2022
Products Sold
1. 8 oz. cartons Lot Code 4212 / Best By Date 11/30/2022; Lot Code 6212 / Best By Date 12/2/2022. EXPANDED 8-10-2022 Lot Code 3102 / Best By Date 08/11/2022. Lot Code 4102 / Best By Date 08/12/2022. Lot Code 7402 / Best By Date 09/14/2022. Lot Code 8402 / Best By Date 09/15/2022. Lot Code 8602 / Best By Date 10/05/2022. Lot Code 9202 / Best By Date 08/27/2022. Lot Code 9602 / Best By Date 10/06/2022. 2. 32 oz. cartons Lot Code 5902 / Best By Date 11/01/2022. Lot Code 6902 / Best By Date 11/02/2022. Lot Code 7212 / Best By Date 12/03/2022. EXPANDED 8-10-2022 Lot Code 0402 / Best By Date 09/07/2022. Lot Code 1702 / Best By Date 10/08/2022. Lot Code 2702 / Best By Date 10/09/2022.
Lyons Magnus, Inc is recalling Sysco Imperial Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Made with 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