RecallHawk
Class II Recall

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

Tipp Distributors, Inc. dba Novamex

Summary

The FDA issued a Class II for Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton by Tipp Distributors, Inc. dba Novamex. Reason: The hermetic seal on the lid of the cans may be compromised.

Details

Source

Food Recall

External ID

F-0264-2025

Action Date

2024-12-18

Status

Ongoing

Category

food

Product Description

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

Lot/Code Info: All lot codes

Quantity Affected: 169,438 cases (2,033,256 cans)

Reason for Recall

The hermetic seal on the lid of the cans may be compromised

Distribution

Only in the US. States: AL, AR, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NY, OH, OK, PA, SC, TN, TX, VA, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-04

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 63 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 II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 "F-0264-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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