FG60007 Green Reviver Juice - point of service product
Summary
The FDA issued a Class II for FG60007 Green Reviver Juice - point of service product by AND GO CONCEPTS DBA SALAD AND GO. Reason: The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations.
Details
Source
Food Recall
External ID
H-0494-2025
Action Date
2025-08-20
Status
Terminated
Category
food
Product Description
FG60007 Green Reviver Juice - point of service product
Lot/Code Info: All lot codes
Quantity Affected: 1,932 bags (4.45lbs per bag)
Reason for Recall
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution
Arizona, Oklahoma, Nevada, Texas
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-27
Company
Garland, TX
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 113 food recalls issued in the same week, part of 204 food-related FDA actions this month.
AND GO CONCEPTS DBA SALAD AND GO has 12 FDA actions in our database, including 12 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 (AND GO CONCEPTS DBA SALAD AND GO) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does AND GO CONCEPTS DBA SALAD AND GO have FDA actions?
AND GO CONCEPTS DBA SALAD AND GO has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0494-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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