Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.; Serv
Summary
The FDA issued a Class III for Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ing by Tiffany Food Corp. Reason: Unapproved dye Ponceau 4R.
Details
Source
Food Recall
External ID
H-1387-2026
Action Date
2026-09-23
Status
Ongoing
Category
food
Product Description
Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.; Serving suggestion: ready to eat. Storage: keep in cool and dry place and keep tightly closed in refrigerator after opening.; PRODUCT OF CHINA; UPC 6 920603 810025
Lot/Code Info: Best Before 10/01/2026
Quantity Affected: 38 cartons
Reason for Recall
Unapproved dye Ponceau 4R
Distribution
AZ, NY, CA, FL, GA, IL, MA, MN, NC, NJ, OH, PA, NY, TN, TX, VA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-28
Company
Brooklyn, NY
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 54 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Tiffany Food Corp has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Tiffany Food Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tiffany Food Corp have FDA actions?
Tiffany Food Corp has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1387-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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