RecallHawk
Class III Recall

1964 Zephyrhills 100% Natural Spring Water 16.9 FL Oz (500 mL)

BLUE TRITON

Summary

The FDA issued a Class III for 1964 Zephyrhills 100% Natural Spring Water 16.9 FL Oz (500 mL) by BLUE TRITON. Reason: Bromate in finished product exceeds the MCL of 10ppb..

Details

Source

Food Recall

External ID

F-1422-2023

Action Date

2023-08-23

Status

Terminated

Category

food

Product Description

1964 Zephyrhills 100% Natural Spring Water 16.9 FL Oz (500 mL)

Lot/Code Info: Batch Code Expiry Date 3177WF23E6 12/31/2024 3177WF23E1 12/31/2024 3180WF23E1 12/31/2024 3181WF23E6 12/31/2024 3181WF23E1 12/31/2024 3182WF23E6 1/31/2025 3182WF23E1 1/31/2025 3184wf23e2 1/31/2025 3184WF23E6 1/31/2025 3185wf23e1 1/31/2025 3185WF23E2 1/31/2025 3185WF23E6 1/31/2025 3185WF23E7 1/31/2025 3186WF23E1 1/31/2025 3186WF23E6 1/31/2025 3187WF23E1 1/31/2025 3187WF23E6 1/31/2025 3188WF23E1 1/31/2025 3188WF23E6 1/31/2025 3189WF23E1 1/31/2025 3189WF23E6 1/31/2025 3189WF23E7 1/31/2025 3190WF23E1 1/31/2025 3190WF23E7 1/31/2025

Quantity Affected: 304,470 cases total: 24pk Zephyrhills Spring Water - 190,662 cases and 40pk Zephyrhills Spring Water - 113,808 cases

Reason for Recall

Bromate in finished product exceeds the MCL of 10ppb.

Distribution

Domestic distribution only.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-14

Company

BLUE TRITON

Zephyrhills, FL

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

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 (BLUE TRITON) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does BLUE TRITON have FDA actions?

This is the only FDA action we have on record for BLUE TRITON in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1422-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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