RecallHawk
Class III Recall

LION Pineapple Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per case

3rd Day Beverages LLC

Summary

The FDA issued a Class III for LION Pineapple Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, by 3rd Day Beverages LLC. Reason: Potential contamination with floating objects.

Details

Source

Food Recall

External ID

H-0276-2025

Action Date

2025-07-23

Status

Terminated

Category

food

Product Description

LION Pineapple Spring Water Hydration Drink, 20 fl. oz, packaged in PET bottles, packed 12 per case

Lot/Code Info: UPC/Product Number: 198715474572; Batch Numbers: 25121 through 25128; Best By 05/26

Quantity Affected: 41 cases

Reason for Recall

Potential contamination with floating objects

Distribution

Product was distributed to three (3) retailers in: TN

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-11

Company

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 98 food recalls issued in the same week, part of 204 food-related FDA actions this month.

3rd Day Beverages LLC has 4 FDA actions in our database, including 4 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 (3rd Day Beverages LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does 3rd Day Beverages LLC have FDA actions?

3rd Day Beverages LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0276-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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