Rejuvenate Muscle Health+ 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
Rejuvenate Muscle Health+ Vanilla. 11 fl oz. (330mL) UPC 6 29046-50402 2. Serve Cold, shake well. Manufactured exclusively for Element Nutrition, Ltd., 1887 Whitney Mesa Dr. #6020, Henderson, NV 89014. 4-count Case UPC 629046544028.
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
EXPANDED 8-10-2022 Lot Code 0011 / Best By Date 10/02/2022 Lot Code 0021 / Best By Date 01/10/2023 Lot Code 1011 / Best By Date 10/03/2022 Lot Code 1021 / Best By Date 01/11/2023 Lot Code 3602 / Best By Date 08/26/2023 Lot Code 4602 / Best By Date 08/27/2023 Lot Code 5602 / Best By Date 08/28/2023 Lot Code 6602 / Best By Date 08/29/2023 Lot Code 6911 / Best By Date 01/06/2023 Lot Code 7111 / Best By Date 10/19/2022 Lot Code 7911 / Best By Date 01/07/2023 Lot Code 8111 / Best By Date 10/20/2022 Lot Code 8911 / Best By Date 01/08/2023 Lot Code 9111 / Best By Date 10/21/2022 Lot Code 9901 / Best By Date 10/01/2022 Lot Code 9911 / Best By Date 01/09/2023
Lyons Magnus, Inc is recalling Rejuvenate Muscle Health+ Vanilla. 11 fl oz. (330mL) UPC 6 29046-50402 2. Serve Cold, shake well. 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