RecallHawk
Class II Recall

FG60007 Green Reviver Juice - point of service product

AND GO CONCEPTS DBA SALAD AND GO

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

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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