Summary
The FDA issued a Class II for Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case) by Victor Packing Inc.. Reason: Misbranded - label states 2g total carbohydrates instead of 27g.
Details
Source
Food Recall
External ID
F-0718-2025
Action Date
2025-04-16
Status
Ongoing
Category
food
Product Description
Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case)
Lot/Code Info: Lot numbers: 255123024, 255123124, 255010225, 255010425, 225010625, 255011725, 255011825, 255012025, 255012125, 255012225, 255012325, 255012425, 255012525, 255012625, 255012725, 255012825, 255012925, 255013025, 255020525, 255022625, 255020725, 255021225, 255021325, 255021725, 255021825
Quantity Affected: 34,500 cases
Reason for Recall
Misbranded - label states 2g total carbohydrates instead of 27g
Distribution
MA, NC, IL, WI, TX, CA, MD, OK, FL
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-17
Company
Madera, CA
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.
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 (Victor Packing Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Victor Packing Inc. have FDA actions?
This is the only FDA action we have on record for Victor Packing Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0718-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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