C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
Summary
The FDA issued a Class III for C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8 by Tipp Distributors, Inc. dba Novamex. Reason: The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (.
Details
Source
Food Recall
External ID
H-0545-2026
Action Date
2026-03-18
Status
Ongoing
Category
food
Product Description
C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
Lot/Code Info: Expiry 4/3/2027 to 6/5/2027
Quantity Affected: 12,000 Cases
Reason for Recall
The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (5g per 17.5oz can), while the primary packaging (the can) has the correct Nutrition Facts Panel and Ingredient List.
Distribution
CO, CA, AZ, WA, TX, FL, IL, MO, NJ, MN, MI
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-25
Company
El Paso, TX
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 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tipp Distributors, Inc. dba Novamex has 2 FDA actions in our database, including 2 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 (Tipp Distributors, Inc. dba Novamex) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tipp Distributors, Inc. dba Novamex have FDA actions?
Tipp Distributors, Inc. dba Novamex has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0545-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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