RecallRadar
ModerateReported December 10, 2025

Aojia Dried Red Bayberry

Recalled by Rong Shing Trading NY Inc

Food recall

Rong Shing Trading NY Inc

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

See all recalls involving an undeclared allergen

Rong Shing Trading NY Inc has recalled Aojia Dried Red Bayberry, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 10, 2025 and was initiated on October 9, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Aojia Dried Red Bayberry, with approximately 10 cases affected. The company behind the recall is Rong Shing Trading NY Inc, based in Brooklyn, NY. The FDA describes the product as: “Aojia Dried Red Bayberry; packaged in 5.6oz (160g) clear plastic bottle; UPC 6942514920327”

Why was Aojia Dried Red Bayberry recalled?

According to the FDA, the stated reason for the recall is: “Product contains undeclared sulfites (7.39mg/serving) and cyclamates.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Aojia Dried Red Bayberry, compare it against the product description and identifying codes (Expiration: 05/19/2026) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Rong Shing Trading NY Inc or your local health authority.

About this recall

This recall was distributed in NY. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
December 10, 2025
Recall started
October 9, 2025
Distributed in
NY
What was recalled
Aojia Dried Red Bayberry; packaged in 5.6oz (160g) clear plastic bottle; UPC 6942514920327
Why it was recalled (as stated by the FDA)
Product contains undeclared sulfites (7.39mg/serving) and cyclamates
How to identify the affected product
Expiration: 05/19/2026
Amount recalled
10 cases

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Aojia Dried Red Bayberry recalled?+

According to the FDA: Product contains undeclared sulfites (7.39mg/serving) and cyclamates

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Aojia Dried Red Bayberry?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0247-2026. Information last synced from the FDA on July 5, 2026.