Yoder's Cashew Crunch Corn, bulk candy coated popcorn packaged in clear plastic without label.
Summary
The FDA issued a Class II for Yoder's Cashew Crunch Corn, bulk candy coated popcorn packaged in clear plastic by Yoder's Cashew Crunch. Reason: Undeclared allergen labeling (milk).
Details
Source
Food Recall
External ID
F-0297-2025
Action Date
2024-12-25
Status
Terminated
Category
food
Product Description
Yoder's Cashew Crunch Corn, bulk candy coated popcorn packaged in clear plastic without label.
Lot/Code Info: No coding system in place
Quantity Affected: 138.92 pounds
Reason for Recall
Undeclared allergen labeling (milk)
Distribution
Distributed to retail and wholesale in: IA and GA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-04
Company
Riverside, IA
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 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Yoder's Cashew Crunch has 5 FDA actions in our database, including 5 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 (Yoder's Cashew Crunch) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Yoder's Cashew Crunch have FDA actions?
Yoder's Cashew Crunch has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0297-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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