RecallHawk
Class I Recall

NuGo Dark Chocolate Chip, Real Dark Chocolate / Vegan. 12g Protein

Bazzini LLC

Summary

The FDA issued a Class I for NuGo Dark Chocolate Chip, Real Dark Chocolate / Vegan. 12g Protein by Bazzini LLC. Reason: The product is being recalled because of undeclared milk ..

Details

Source

Food Recall

External ID

F-0462-2025

Action Date

2025-02-12

Status

Terminated

Category

food

Product Description

NuGo Dark Chocolate Chip, Real Dark Chocolate / Vegan. 12g Protein

Lot/Code Info: 52192 Best By 21 Dec 2025 C24234B Nugo Dark Chocolate Chocolate Chip 52192 Best By 22 Dec 2025 C24235A Nugo Dark Chocolate Chocolate Chip 52192 Best By 22 Dec 2025 C24235B Nugo Dark Chocolate Chocolate Chip 52192 Best By 23 Dec 2025 C24236A Nugo Dark Chocolate Chocolate Chip

Quantity Affected: 223,872 bars

Reason for Recall

The product is being recalled because of undeclared milk .

Distribution

The recalled product was distributed to the following states NC, MS, MA,ME, IL, PA, IA, GA, FL, MD, NJ, VA, MA, WA,

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-27

Company

Bazzini LLC

Allentown, PA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Bazzini LLC has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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

How often does Bazzini LLC have FDA actions?

Bazzini LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0462-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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