Prosperity Resources International Mixed Fruit Candy Recall

Why it was recalled

Prosperity Resources is recalling Sun Kee Mixed Fruit Candy because sampling analysis revealed it contains undeclared colors, FD&C Blue #1, Red #40, Yellow #5 and #6 and the product also contains an unallowable dye: 16185 - Amaranth (E123) - delisted FD&C Red #2

Product description

Mixed Fruit Candy, Net Wt. 12 oz. (340g), Distributed by: Prosperity Resources Int'l, Inc., Product of China, UPC 6 47406 02091 3

Lot numbers, UPCs & expiration codes

N/A

Where it was sold

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-3250-2015
Classification: Class II
Status: Terminated
Recall initiated: Aug 3, 2015
FDA report date: Oct 7, 2015
Quantity: 96 bags
Recall type: Voluntary: Firm initiated
Recalling firm: Prosperity Resources International, Inc.

Original FDA data

Every field from FDA enforcement report F-3250-2015, exactly as published.

Show all FDA fields

City: Linden
State: NJ
Status: Terminated
Country: United States
Event ID: 71997
Address: 1080 Edward St
Postal code: 07036-6408
Report date: Oct 7, 2015
Product type: Food
Recall number: F-3250-2015
Classification: Class II
Recalling firm: Prosperity Resources International, Inc.
Product quantity: 96 bags
Termination date: Jun 1, 2017
Reason for recall: Prosperity Resources is recalling Sun Kee Mixed Fruit Candy because sampling analysis revealed it contains undeclared colors, FD&C Blue #1, Red #40, Yellow #5 and #6 and the product also contains an unallowable dye: 16185 - Amaranth (E123) - delisted FD&C Red #2
Voluntary / mandated: Voluntary: Firm initiated
Product description: Mixed Fruit Candy, Net Wt. 12 oz. (340g), Distributed by: Prosperity Resources Int'l, Inc., Product of China, UPC 6 47406 02091 3
Distribution pattern: NY
Recall initiation date: Aug 3, 2015
Initial firm notification: Letter
Center classification date: Sep 28, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-3250-2015, published Oct 7, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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