RecallHawk
Class II Recall

5000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough, 8 poly bags of 18 frozen pucks in a corrugate case, Net Weight

Craftmark Bakery, LLC

Summary

The FDA issued a Class II for 5000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough, 8 poly bags of 18 froze by Craftmark Bakery, LLC. Reason: Potential contamination with foreign material (plastic).

Details

Source

Food Recall

External ID

F-0690-2025

Action Date

2025-04-09

Status

Terminated

Category

food

Product Description

5000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough, 8 poly bags of 18 frozen pucks in a corrugate case, Net Weight 27.00 lb

Lot/Code Info: 5A057

Quantity Affected: 119 cases

Reason for Recall

Potential contamination with foreign material (plastic)

Distribution

CA, IL, MD, CANADA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-27

Company

Craftmark Bakery, LLC

Indianapolis, IN

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

Craftmark Bakery, LLC has 4 FDA actions in our database, including 4 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 (Craftmark Bakery, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Craftmark Bakery, LLC have FDA actions?

Craftmark Bakery, LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0690-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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