RecallHawk
Class II Recall

CaBOT CREAMERY SEA SALT CARAMEL CHEDDAR SWEET & CHEESY POPCORN 6.0oz bag CONTAINS: SOY & MILK UPC 8 50016 94430 6 MANUFA

Jody's Inc.

Summary

The FDA issued a Class II for CaBOT CREAMERY SEA SALT CARAMEL CHEDDAR SWEET & CHEESY POPCORN 6.0oz bag CONTAIN by Jody's Inc.. Reason: Undeclared Peanuts. The firm received two complaints that the product contains peanuts which are not listed in the ingredient statement..

Details

Source

Food Recall

External ID

H-0139-2026

Action Date

2025-11-05

Status

Ongoing

Category

food

Product Description

CaBOT CREAMERY SEA SALT CARAMEL CHEDDAR SWEET & CHEESY POPCORN 6.0oz bag CONTAINS: SOY & MILK UPC 8 50016 94430 6 MANUFACTURED FOR: VERMONT CHEESE PRODUCTS, INC 60 LAKE STREET, SUITE 2A BURLINGTON, VT 05401

Lot/Code Info: Lot 2519907B1 BEST IF ENJOYED BY: 07 15 26

Quantity Affected: 8,244 units

Reason for Recall

Undeclared Peanuts. The firm received two complaints that the product contains peanuts which are not listed in the ingredient statement.

Distribution

Product was shipped to one distribution center in IL.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-17

Company

Jody's Inc.

Norfolk, VA

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 62 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 (Jody's Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Jody's Inc. have FDA actions?

This is the only FDA action we have on record for Jody's Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0139-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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