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Class ITerminated in FDA datasetRecall initiated Jun 9, 2023

Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12153

Recalling firm: Richin Trading Inc

Why it was recalled

Potential choking hazard

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 13, 2023.

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Compare the exact product and package details with the label you have.

ProductSun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12153; UPC 715685121536; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12144; UPC 715685121444; Net Weight 52.91 oz. (1500 g)
Package size35.27 oz
UPC715685121444, 715685121536

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12153; UPC 715685121536; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12144; UPC 715685121444; Net Weight 52.91 oz. (1500 g)

Extracted codes and context

TypeCode / valueContext
UPC715685121444Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12144; UPC 715685121444; Net Weight 52.91 oz. (1500 g)
UPC715685121536Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12153; UPC 715685121536; Net Weight 35.27 oz. (1000 g) Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12144; UPC 715685

Original FDA recall reason

Potential choking hazard

Recall details

Recall number
F-1300-2023
Event ID
92538
FDA status
Terminated
Initiated
Jun 9, 2023
Reported
Jul 5, 2023
Classified
Jul 31, 2023
Terminated
Oct 13, 2023
Quantity
141,192 units total
Location
Alhambra, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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

FDA source record · F-1300-2023

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.