CLASS I Food recall · Reported 1 Jul 2020 · FDA Enforcement Report

Xi Zhi Liang Fruit Jelly Cups recalled by Rong Shing Trading NY

Rong Shing Trading NY is recalling Xi Zhi Liang Fruit Jelly Cups, distributed in Illinois, Minnesota, New York, Pennsylvania, Virginia. The recall was initiated on 11 Jun 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBEST BEFORE 12.30.2020; UPC 6902934982123
Quantity recalled65 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
F-1000-2020
FDA event ID
85845
Recalling firm
Rong Shing Trading NY, Brooklyn, NY
Brand
Xi Zhi
Classification
Class I
Status
Terminated
Recall initiated
11 Jun 2020
FDA classified
23 Jun 2020
Reported
1 Jul 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Choking Hazard
Product category
Jam & Jelly

Timeline

11 Jun 2020Recall initiated by company
23 Jun 2020Classified by FDA+12 days
1 Jul 2020Published in enforcement report+8 days

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

Reason for recall

The product presents a significant choking hazard.

Product as listed by the FDA

Xi Zhi Liang Fruit Jelly Cups; 21.1oz (600g); packaged in pink, yellow, and blue plastic backpacks with numerous individual plastic jelly cups inside each backpack and a toy car in a pouch on the front of the plastic backpack; the product contains konjac powder

Where it was distributed

VA, MN, NY, IL, PA

IllinoisMinnesotaNew YorkPennsylvaniaVirginia

Questions about this recall

Why was it recalled?

The product presents a significant choking hazard.

Which lots are affected?

BEST BEFORE 12.30.2020; UPC 6902934982123

Where was it sold?

VA, MN, NY, IL, PA

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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