RecallHawk
Class II Recall

Chicago Sweet Connections: Coffee Cake - Custard Flavor packaged in an aluminum rectangular tray with plastic dome lid S

Chicago Sweet Connections, Inc.

Summary

The FDA issued a Class II for Chicago Sweet Connections: Coffee Cake - Custard Flavor packaged in an aluminum by Chicago Sweet Connections, Inc.. Reason: Undeclared Allergens - Egg, Milk, and Wheat.

Details

Source

Food Recall

External ID

F-0847-2022

Action Date

2022-03-16

Status

Terminated

Category

food

Product Description

Chicago Sweet Connections: Coffee Cake - Custard Flavor packaged in an aluminum rectangular tray with plastic dome lid Single pack - 6 servings

Lot/Code Info: UPC 84104904610

Quantity Affected: 11

Reason for Recall

Undeclared Allergens - Egg, Milk, and Wheat

Distribution

Retail locations in IL and WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-25

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

Chicago Sweet Connections, Inc. has 20 FDA actions in our database, including 20 recalls.

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 (Chicago Sweet Connections, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Chicago Sweet Connections, Inc. have FDA actions?

Chicago Sweet Connections, Inc. has 20 FDA actions in our database, including 20 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0847-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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