RecallHawk
Class II Recall

Bake Crafters - Maple Waffle WG Chicken Sausage Packaged into cardboard containers 126 units per case

Bake Crafters

Summary

The FDA issued a Class II for Bake Crafters - Maple Waffle WG Chicken Sausage Packaged into cardboard contain by Bake Crafters. Reason: Potential Listeria monocytogenes contamination.

Details

Source

Food Recall

External ID

F-0620-2022

Action Date

2022-02-02

Status

Terminated

Category

food

Product Description

Bake Crafters - Maple Waffle WG Chicken Sausage Packaged into cardboard containers 126 units per case

Lot/Code Info: Lot Number: 21343 Product Number: 6657 Best By: 12/09/22

Quantity Affected: 162 cases

Reason for Recall

Potential Listeria monocytogenes contamination

Distribution

Distributed to Distribution Centers in ID and PA

Type: Voluntary: Firm initiated

Recall Initiated: 2021-12-28

Company

Bake Crafters

Mc Donald, TN

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

How often does Bake Crafters have FDA actions?

This is the only FDA action we have on record for Bake Crafters in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0620-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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