Class II Recall

Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: 1.2 oz / 35gr. No UP

Summary

The FDA issued a Class II for Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue by Cocanu LLC. Reason: Lactose is declared but milk is not declared on label..

Details

Source

Food Recall

External ID

F-0867-2021

Action Date

2021-08-25

Status

Terminated

Product Description

Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: 1.2 oz / 35gr. No UPC. The label is read in parts: "***Moonwalk ***a 70% dark chocolate bar ***chocolate, cacao nibs and pop rocks ***Contents: cacao beans, cacao butter, cane sugar, pop rocks (sugar, lactose, corn syrup, flavoring)***cloudforest Portland, OR***cloudforest.shop***".

Lot/Code Info: Lot 683 (Best by 8/26/2021) Lot 690 (Best by 12/15/2021) Lot 695 (Best by 12/30/2021) Lot 703 (Best by 2/11/2022) Lot 709 (Best by 3/10/2022) Lot 722 (Best by 5/28/2022)

Quantity Affected: 852 bars

Reason for Recall

Lactose is declared but milk is not declared on label.

Distribution

Distributed in CA and OR.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-08-03

Company

Cocanu LLC

Portland, OR

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

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

How often does Cocanu LLC have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0867-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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