RecallHawk
Class II Recall

Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627

Wilton Industries Inc

Summary

The FDA issued a Class II for Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627 by Wilton Industries Inc. Reason: Milk contamination.

Details

Source

Food Recall

External ID

F-1384-2022

Action Date

2022-07-06

Status

Terminated

Category

food

Product Description

Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627

Lot/Code Info: lots 21005Z and 21111Z

Quantity Affected: 16281 units

Reason for Recall

Milk contamination

Distribution

Nationwide US. Exported to: Panama Honduras Aruba Mexico

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-02

Company

Wilton Industries Inc

Naperville, IL

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

Wilton Industries Inc has 3 FDA actions in our database, including 3 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 (Wilton Industries Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wilton Industries Inc have FDA actions?

Wilton Industries Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1384-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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