RecallHawk
Class III Recall

The label reads, "Golden Sunrise Cold Pressured Juice Carrot, Orange, Pineapple, Lemon, Ginger & Turmeric 11 fl. oz."

Pressery, LLC

Summary

The FDA issued a Class III for The label reads, "Golden Sunrise Cold Pressured Juice Carrot, Orange, Pineapple, by Pressery, LLC. Reason: Bottle of juice was found at the store level with the incorrect sku label..

Details

Source

Food Recall

External ID

F-1095-2024

Action Date

2024-04-03

Status

Terminated

Category

food

Product Description

The label reads, "Golden Sunrise Cold Pressured Juice Carrot, Orange, Pineapple, Lemon, Ginger & Turmeric 11 fl. oz."

Lot/Code Info: UPC: 0-99482-53091-4 Lot code: MFG on: 01/09/24 WGS

Quantity Affected: 57 cases: 12 bottles per case: 684 bottles

Reason for Recall

Bottle of juice was found at the store level with the incorrect sku label.

Distribution

Distributed to retail stores throughout the U.S.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-16

Company

Pressery, LLC

Denver, CO

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

How often does Pressery, LLC have FDA actions?

This is the only FDA action we have on record for Pressery, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1095-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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