CriticalClass ITerminated

FDA Food recall · Reported July 5, 2023

Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 715685121529; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12145; UPC 715685121451; Net Weight 52.91 oz. (1500 g)

Q: Which agency issued this recall?

This recall was issued by the FDA Food on July 5, 2023. Severity: Critical. Recall number: F-1301-2023.

Q: Where was the recalled product distributed?

Distribution: Distributed to locations in AZ, CA, CO, GA, HI, IA, KS, MA, MD, MN, NJ, NV, OR, PA, TX, UT, WA.

Q: What are the health risks of consuming a recalled food product?

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Potential choking hazard

Recall #: F-1301-2023
Affected scope: 141,192 units total
Initiated: June 9, 2023

Compiled from official public sources by the publisher. · Updated September 2026

Verify with FDA Food →

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Richin Trading Inc recalled Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 71568512… - a critical-severity action.

Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 71568512… was recalled by Richin Trading Inc in July 5, 2023. Reason: Potential choking hazard. Check the official notice for the remedy. Verify recall #F-1301-2023 with the FDA Food before acting.

The recall

Richin Trading Inc issued this critical-severity FDA Food recall-Potential choking hazard.

Critical
severity level: 141K units
affected scope: Class I
classification: July 5, 2023
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1301-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope (see the Recall Profile below) is large enough to require multi-state distribution tracking. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 715685121529; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12145; UPC 715685121451; Net Weight 52.91 oz. (1500 g)

Reason for recall

Potential choking hazard

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Critical (Class I)
Status	Terminated
Recall number	F-1301-2023
Date reported	July 5, 2023
Date initiated	June 9, 2023
Recalling firm	Richin Trading Inc
Firm location	Alhambra, CA
Affected scope	141,192 units total
Distribution	Distributed to locations in AZ, CA, CO, GA, HI, IA, KS, MA, MD, MN, NJ, NV, OR, PA, TX, UT, WA

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

141,192 units total units affected - multi-state distribution scale.

Regional (<10K units) -

Multi-state (10K – 100K units) -

Large-scale (100K – 1M units) ✓ This recall

Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-1301-2023) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

Potential choking hazard

Which agency issued this recall? ▼

This recall was issued by the FDA Food on July 5, 2023. Severity: Critical. Recall number: F-1301-2023.

Where was the recalled product distributed? ▼

Distribution: Distributed to locations in AZ, CA, CO, GA, HI, IA, KS, MA, MD, MN, NJ, NV, OR, PA, TX, UT, WA.

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Critical), closest by report date among other firms and states.

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Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported July 5, 2023. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026