Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 715685121529; Net Weight 35.27 oz. (100
Summary
The FDA issued a Class I for Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC by Richin Trading Inc. Reason: Potential choking hazard.
Details
Source
Food Recall
External ID
F-1301-2023
Action Date
2023-07-05
Status
Terminated
Category
food
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)
Lot/Code Info: Lot # Exp Date 74602007 6/13/2024 74432004 6/6/2024 74081991 5/24/2024 74201994 3/9/2024 74071990 5/2/2024 73871986 4/19/2024 73861985 2/3/2024 73891988 1/29/2024 73811984 1/11/2024 73561223 11/27/2023 73561123 11/17/2023 71980823 10/2/2023 72541123 11/10/2023 72530623 7/14/2023
Quantity Affected: 141,192 units total
Reason for Recall
Potential choking hazard
Distribution
Distributed to locations in AZ, CA, CO, GA, HI, IA, KS, MA, MD, MN, NJ, NV, OR, PA, TX, UT, WA
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-09
Company
Alhambra, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 23 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Richin Trading Inc has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Richin Trading Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Richin Trading Inc have FDA actions?
Richin Trading Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1301-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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