Class I Recall

Lyons Barista Style Oat, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10180 7. 12 count

Summary

The FDA issued a Class I for Lyons Barista Style Oat, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) by Lyons Magnus, Inc. Reason: Findings and potential for Cronobacter sakazakii and Clostridium botulinum..

Details

Source

Food Recall

External ID

F-1617-2022

Action Date

2022-09-07

Status

Terminated

Product Description

Lyons Barista Style Oat, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10180 7. 12 count case UPC 10045796101804. Shake Well before Serving. After opening keep refrigerated and use within 7 days. Lyons Magnus, Fresno, CA 93702.

Lot/Code Info: Lot Code 0612 / Best By Date 03/06/2023; Lot Code 2212 / Best By Date 01/27/2023; Lot Code 3212 / Best By Date 01/28/2023; Lot Code 4212 / Best By Date 01/29/2023; Lot Code 6412 / Best By Date 02/20/2023; Lot Code 7412 / Best By Date 02/21/2023. EXPANDED 8-10-2022 Lot Code 0231 / Best By Date 08/13/2022. Lot Code 0902 / Best By Date 12/26/2022. Lot Code 1102 / Best By Date 10/08/2022. Lot Code 1231 / Best By Date 08/14/2022. Lot Code 2102 / Best By Date 10/09/2022. Lot Code 4331 / Best By Date 08/27/2022. Lot Code 4402 / Best By Date11/10/2022. Lot Code 5202 / Best By Date 10/22/2022. Lot Code 5331 / Best By Date 08/28/2022. Lot Code 5402 / Best By Date 11/11/2022. Lot Code 6202 / Best By Date 10/23/2022. Lot Code 6402 / Best By Date 11/12/2022. Lot Code 7202 / Best By Date 10/24/2022. Lot Code 7402 / Best By Date 11/13/2022. Lot Code 8402 / Best By Date 11/14/2022. Lot Code 8802 / Best By Date 12/24/2022. Lot Code 9402 / Best By Date 11/15/2022. Lot Code 9431 / Best By Date 09/11/2022. Lot Code 9802 / Best By Date 12/25/2022.

Quantity Affected: 53,818,025 total units

Reason for Recall

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-22

Company

Lyons Magnus, Inc

Fresno, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lyons Magnus, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lyons Magnus, Inc have FDA actions?

Lyons Magnus, Inc has 78 FDA actions in our database, including 78 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1617-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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