Recalls / Class I
Class IF-1615-2022
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Lyons Barista Style Almond, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10165 4. 12 count case UPC 10045796101651. Shake Well before Serving. After opening keep refrigerated and use within 7 days. Lyons Magnus, Fresno, CA 93702.
- Type
- Food
- Affected lot / code info
- Lot Code 2012 / Best By Date 01/07/2023; Lot Code 3012 / Best By Date 01/08/2023; Lot Code 3712 / Best By Date 03/19/2023; Lot Code 4012 / Best By Date 01/09/2023; Lot Code 5012 / Best By Date 01/10/2023; Lot Code 5712 / Best By Date 03/21/2023. EXPANDED 8-10-2022 Lot Code 0302 / Best By Date 10/27/2022. Lot Code 0531 / Best By Date 09/12/2022. Lot Code 0602 / Best By Date 11/26/2022. Lot Code 1231 / Best By Date 08/14/2022. Lot Code 1302 / Best By Date 10/28/2022. Lot Code 1602 / Best By Date 11/27/2022. Lot Code 2231 / Best By Date 08/15/2022. Lot Code 2302 / Best By Date 10/29/2022. Lot Code 2602 / Best By Date 11/28/2022. Lot Code 3102 / Best By Date 10/10/2022. Lot Code 3231 / Best By Date 08/16/2022. Lot Code 3602 / Best By Date 11/29/2022. Lot Code 4102 / Best By Date 10/11/2022. Lot Code 4602 / Best By Date 11/30/2022. Lot Code 5602 / Best By Date 12/01/2022. Lot Code 9431 / Best By Date 09/11/2022. Lot Code 9502 / Best By Date 11/25/2022.
- Quantity
- 53,818,025 total units
Why it was recalled
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Recalling firm
- Firm
- Lyons Magnus, Inc
- Notification channel
- Telephone
- Type
- Voluntary: Firm initiated
- Address
- 3158 E Hamilton Ave, Fresno, California 93702-4163
Distribution
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2022-07-22
- FDA classified
- 2022-08-30
- Posted by FDA
- 2022-09-07
- Terminated
- 2024-07-25
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1615-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.