Lyons Ready Care Thickened Dairy Drink (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 Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Grade A Made with 2% Milk Fat Milk, Vitamins A & D Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 45796-10044 2. Item 10044. 24 count case UPC 10045796100449. 2. 32 FL OZ (1 QT) 946mL UPC 0 45796-10046 6. Item 10046. 12 count case UPC 10045796100463. Refrigerate after opening. Manufactured for Lyons Magnus, Fresno, CA 93702.
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
Lot Code 5512 / Best By Date 12/31/2022
Products Sold
1. 8 oz. containers: Lot Code 0012 / Best By Date 11/06/2022. EXPANDED 8-10-2022 Lot Code 0102 / Best By Date 08/08/2022. Lot Code 4102 / Best By Date 08/12/2022. Lot Code 5102 / Best By Date 08/13/2022. Lot Code 6402 / Best By Date 09/13/2022. Lot Code 7402 / Best By Date 09/14/2022. Lot Code 8202 / Best By Date 08/26/2022. 2. 32 oz. containers: Lot Code 4512 / Best By Date 12/30/2022; Lot Code 5512 / Best By Date 12/31/2022; Lot Code 5902 / Best By Date 11/01/2022. EXPANDED 8-10-2022 Lot Code 1702 / Best By Date 10/08/2022.
Lyons Magnus, Inc is recalling Lyons Ready Care Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Grade 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