Premier Protein Cafe Latte Shake (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
Premier Protein Cafe Latte High protein shake. 11 FL OZ (325mL). Packaged in the following configurations: 1. Carton UPC 6 43843-71668 6 packed in 4 count wrap UPC 643843716679. 2. Carton UPC 6 43843-71665 5 packed in 18 count case UPC 643843718567. Shake Well and Serve Cold. Refrigerate after Opening. Distributed by: Premier Nutrition, Emeryville, CA 94608. EXPANDED 8-10-2022 3. Carton UPC 6 43843-71668 6 Packed in 12 count case UPC 643843716624.
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
1. 4 count case Lot Code 3212/2123BT / Best By Date 7/1/2023, Lot Code 4212/2124BT / Best By Date 7/2/2023, Lot Code 5212/2125BT / Best By Date 7/3/2023, Lot Code 62122126BT / Best By Date 7/4/2023, 12 count case Lot Code 0402 / 2040BT / Best By Date 4/9/2023.
Products Sold
1. 4 count case Lot Code 3212/2123BT / Best By Date 7/1/2023; Lot Code 4212/2124BT / Best By Date 7/2/2023; Lot Code 5212/2125BT / Best By Date 7/3/2023; Lot Code 62122126BT / Best By Date 7/4/2023; Lot Code 7212/2127BT / Best By Date 7/5/2023. 2. 18 count case Lot Code 8212/2128BT / Best By Date 7/6/2023. EXPANDED 8-10-2022 3, 12 count case Lot Code 0402 / 2040BT / Best By Date 4/9/2023.
Lyons Magnus, Inc is recalling Premier Protein Cafe Latte High protein shake. 11 FL OZ (325mL). Packaged in the following con 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