CLASS II Food recall · Reported 10 Dec 2025 · FDA Enforcement Report

Aojia Dried Red Bayberry recalled by Rong Shing Trading NY

Rong Shing Trading NY is recalling Aojia Dried Red Bayberry, distributed in Massachusetts, New Jersey, New York, Virginia. The recall was initiated on 9 Oct 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration: 05/19/2026
Quantity recalled10 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0247-2026
FDA event ID
98008
Recalling firm
Rong Shing Trading NY, Brooklyn, NY
Brand
Aojia
Classification
Class II
Status
Terminated
Recall initiated
9 Oct 2025
FDA classified
9 Dec 2025
Reported
10 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Other

Timeline

9 Oct 2025Recall initiated by company
9 Dec 2025Classified by FDA+61 days
10 Dec 2025Published in enforcement report+1 day

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains undeclared sulfites (7.39mg/serving) and cyclamates

Product as listed by the FDA

Aojia Dried Red Bayberry; packaged in 5.6oz (160g) clear plastic bottle; UPC 6942514920327

Where it was distributed

VA, NJ, MA, NY

MassachusettsNew JerseyNew YorkVirginia

Questions about this recall

Why was it recalled?

Product contains undeclared sulfites (7.39mg/serving) and cyclamates

Which lots are affected?

Expiration: 05/19/2026

Where was it sold?

VA, NJ, MA, NY

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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