RecallHawk
Class III Recall

SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per case.

SHANDONG JOYWIN INTERNATIONAL TRADING CO.,LTD.

Summary

The FDA issued a Class III for SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per by SHANDONG JOYWIN INTERNATIONAL TRADING CO.,LTD.. Reason: Undeclared Red No. 3 (E127)].

Details

Source

Food Recall

External ID

H-0259-2025

Action Date

2025-07-16

Status

Terminated

Category

food

Product Description

SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per case.

Lot/Code Info: R241077 Production Code Date: CAN CODE: 3700/01115 Best by: NOV/26/2027 624 R241079 Production Code Date: CAN CODE: 3700/01115 Best by: DEC/04/2027 624

Quantity Affected: 1105 Cases

Reason for Recall

Undeclared Red No. 3 (E127)]

Distribution

The recalled product was distributed to the following states: IL, PA, FL, AL

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-19

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 147 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (SHANDONG JOYWIN INTERNATIONAL TRADING CO.,LTD.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does SHANDONG JOYWIN INTERNATIONAL TRADING CO.,LTD. have FDA actions?

This is the only FDA action we have on record for SHANDONG JOYWIN INTERNATIONAL TRADING CO.,LTD. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0259-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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