Lyons Ready Care 2.0 Vanilla (Lyons Magnus) – bacterial contamination (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
Lyons Ready Care 2.0 Vanilla High Calorie, High Protein, Nutritional Drink. 32 FL OZ (1 QT) 946mL UPC 0 45796-10091 6 Item 10091. 12 count case UPC 10045796100913. Refrigerate after opening. Lyons Magnus, Fresno, CA 93702.
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
Lot Code 5312 / Best By Date 02/09/2023, Lot Code 6312 / Best By Date 02/10/2023, Lot Code 6512 / Best By Date 03/02/2023, Lot Code 7512 / Best By Date 03/03/2023, Lot Code 8512 / Best By Date 03/04/2023, Lot Code 8902 / Best By Date 01/03/2023
Products Sold
Lot Code 5312 / Best By Date 02/09/2023; Lot Code 6312 / Best By Date 02/10/2023; Lot Code 6512 / Best By Date 03/02/2023; Lot Code 7512 / Best By Date 03/03/2023; Lot Code 8512 / Best By Date 03/04/2023; Lot Code 8902 / Best By Date 01/03/2023; Lot Code 9902 / Best By Date 01/04/2023. EXPANDED 8-10-2022 Lot Code 3302 / Best By Date 10/30/2022. Lot Code 4002 / Best By Date 10/01/2022. Lot Code 4302 / Best By Date 10/31/2022. Lot Code 5002 / Best By Date 10/02/2022.
Lyons Magnus, Inc is recalling Lyons Ready Care 2.0 Vanilla High Calorie, High Protein, Nutritional Drink. 32 FL OZ (1 QT) 946m 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