RecallHawk
Class III Recall

Cotton Blues Cheesecake Co. Strawberry Swirl Single Slice 6oz plastic container 36 packages per case

CB DISTRIBUTION LLC

Summary

The FDA issued a Class III for Cotton Blues Cheesecake Co. Strawberry Swirl Single Slice 6oz plastic container by CB DISTRIBUTION LLC. Reason: Incorrect Ingredient Labeling.

Details

Source

Food Recall

External ID

F-0870-2021

Action Date

2021-08-25

Status

Terminated

Category

food

Product Description

Cotton Blues Cheesecake Co. Strawberry Swirl Single Slice 6oz plastic container 36 packages per case

Lot/Code Info: Product Number 6320400047 Lot Numbers: 4113, 4110, 4128, 4126, 4130, 4121, 4118 Best By Dates: 12/21/22, 12/23/22, 01/01/23, 01/06/23, 01/12/23, 01/14/23, 01/16/23

Quantity Affected: 288 cases

Reason for Recall

Incorrect Ingredient Labeling

Distribution

Product was shipped to distribution centers in Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2021-08-09

Company

CB DISTRIBUTION LLC

Waynesboro, MS

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

How often does CB DISTRIBUTION LLC have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0870-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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