RecallHawk
Class II Recall

Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.

RDK Corp. dba Racine Danish Kringles

Summary

The FDA issued a Class II for Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp by RDK Corp. dba Racine Danish Kringles. Reason: Raspberry Kringle may contain undeclared tree nuts (pecans)..

Details

Source

Food Recall

External ID

F-0711-2024

Action Date

2024-01-10

Status

Terminated

Category

food

Product Description

Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.

Lot/Code Info: Lot code 23299

Quantity Affected: 960 units

Reason for Recall

Raspberry Kringle may contain undeclared tree nuts (pecans).

Distribution

IA, MN, ND, SD, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-18

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 12 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 (RDK Corp. dba Racine Danish Kringles) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does RDK Corp. dba Racine Danish Kringles have FDA actions?

This is the only FDA action we have on record for RDK Corp. dba Racine Danish Kringles in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0711-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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