Food recall
Lyons Magnus LLC recall: Lyons Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
Lyons Magnus LLC, of Fresno, CA, recalled Lyons Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case and 2 other products. The FDA's reason: “Signs of bloating in juice cups.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on August 11, 2023, and the FDA first listed it in its Enforcement Report of September 6, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class II
It could cause temporary or minor harm
Why
Labeling, packaging or manufacturing problems
Status
Terminated
Closed October 2, 2023
The recall
- Company
- Lyons Magnus LLC (Fresno, CA)
- Reason, in FDA's words
- “Signs of bloating in juice cups”
- Where it was sold
- AR, FL, GA, IA, KY, LA, MI, NC, OH, PA, TN TX, WI
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 92872
The 3 products recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-1484-2023 Class II
Lyons Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
Codes: Item No. 5654 Batch Code: 3313, 1613, 7023 Best By: 12/09/23, 01/06/24, 02/21/24
Quantity: 1564 cases
-
F-1485-2023 Class II
GFS Harvest Valley Cranberry/Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
Codes: Item No. 5694 Batch Code: 9213, 1613 Best By: 12/05/23, 01/06/24
Quantity: 1496 cases
-
F-1486-2023 Class II
GFS Harvest Valley Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
Codes: Item No. 5695 Batch Code: 2313, 3313, 1613 Best By: 12/08/23, 12/09/23, 01/06/24
Quantity: 3712 cases
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of September 6, 2023.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.