RecallHawk
Class II Recall

5 oz 2pk Chocolate Croissant, bakery box with clear top (UPC 7789050655) and Chocolate Croissant 2 oz, bakery box with c

Wegmans Food Markets, Inc.

Summary

The FDA issued a Class II for 5 oz 2pk Chocolate Croissant, bakery box with clear top (UPC 7789050655) and Cho by Wegmans Food Markets, Inc.. Reason: Product contains undeclared soy lecithin..

Details

Source

Food Recall

External ID

F-0860-2024

Action Date

2024-02-14

Status

Terminated

Category

food

Product Description

5 oz 2pk Chocolate Croissant, bakery box with clear top (UPC 7789050655) and Chocolate Croissant 2 oz, bakery box with clear top (UPC 7789048398)

Lot/Code Info: Best By Dates: To be provided ASAP

Quantity Affected: 10,338 croissants Total

Reason for Recall

Product contains undeclared soy lecithin.

Distribution

NY, VA, MD, PA, NJ, MA, NC, DE, DC

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-12

Company

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

Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 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 (Wegmans Food Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wegmans Food Markets, Inc. have FDA actions?

Wegmans Food Markets, Inc. has 28 FDA actions in our database, including 28 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0860-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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