Skip to main content
RecallFDAfda-H-0545-2026OTHER

C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8

Category
Units Affected
12,000
Recall Date
February 25, 2026
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0545-2026.

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.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0545-2026.

Recall ongoing. Follow firm instructions.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Tipp Distributors, Inc. Dba Novamex or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0545-2026.

Tipp Distributors, Inc. dba Novamex

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Tipp Distributors, Inc. Dba Novamex Recall FAQ

Tipp Distributors, Inc. Dba Novamex is the subject of a beverages safety report: C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8. The notice was published on February 25, 2026 by the U.S. Food and Drug Administration (FDA). Approximately 12,000 units are potentially affected.