GFS Harvest Valley Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
Summary
The FDA issued a Class II for GFS Harvest Valley Grape Juice packaged in 4 fl oz opaque white plastic cup 96 c by Lyons Magnus LLC. Reason: Signs of bloating in juice cups.
Details
Source
Food Recall
External ID
F-1486-2023
Action Date
2023-09-06
Status
Terminated
Category
food
Product Description
GFS Harvest Valley Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case
Lot/Code Info: Item No. 5695 Batch Code: 2313, 3313, 1613 Best By: 12/08/23, 12/09/23, 01/06/24
Quantity Affected: 3712 cases
Reason for Recall
Signs of bloating in juice cups
Distribution
AR, FL, GA, IA, KY, LA, MI, NC, OH, PA, TN TX, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-11
Company
Fresno, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lyons Magnus LLC has 26 FDA actions in our database, including 26 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 LLC) 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 LLC have FDA actions?
Lyons Magnus LLC has 26 FDA actions in our database, including 26 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1486-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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