RecallHawk
Class III Recall

LEMON PLUM; NET WT: 228G (8oz); INGREDIENTS: Plum, sugar, salt, lemon juice, food additives (citric acid, sodium benzoat

Rong Shing Trading NY Inc

Summary

The FDA issued a Class III for LEMON PLUM; NET WT: 228G (8oz); INGREDIENTS: Plum, sugar, salt, lemon juice, foo by Rong Shing Trading NY Inc. Reason: Product contains cyclamates..

Details

Source

Food Recall

External ID

F-0712-2025

Action Date

2025-04-23

Status

Terminated

Category

food

Product Description

LEMON PLUM; NET WT: 228G (8oz); INGREDIENTS: Plum, sugar, salt, lemon juice, food additives (citric acid, sodium benzoate, potassium sorbate, ethyl maltol, FD&C YELLOW#6, vanillin, saccharin sodium, sodium metabisulfite), food flavoring; DISTRIBUTED BY RONG SHING TRADING NY INC; UPC: 6922300667599

Lot/Code Info: Manufacturing date: 2024/10/10 Best Before date: 10/09/2025

Quantity Affected: 21 cases

Reason for Recall

Product contains cyclamates.

Distribution

NJ, NY, MD, VA, MA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-02-07

Company

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 25 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Rong Shing Trading NY Inc has 6 FDA actions in our database, including 6 recalls.

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 (Rong Shing Trading NY Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Rong Shing Trading NY Inc have FDA actions?

Rong Shing Trading NY Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0712-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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