RecallHawk
Class II Recall

Westby Pepper Cheese Curds, 12 oz. (340g) UPC 7 50388-30105 2. Keep Refrigerated. No Added Preservatives. Manufactur

Westby Cooperative Creamery

Summary

The FDA issued a Class II for Westby Pepper Cheese Curds, 12 oz. (340g) UPC 7 50388-30105 2. Keep Refrigerat by Westby Cooperative Creamery. Reason: Cheese curds may be contaminated with generic E. coli..

Details

Source

Food Recall

External ID

F-0125-2025

Action Date

2024-11-20

Status

Terminated

Category

food

Product Description

Westby Pepper Cheese Curds, 12 oz. (340g) UPC 7 50388-30105 2. Keep Refrigerated. No Added Preservatives. Manufactured by Westby Cooperative Creamery, Westby, WI 54667.

Lot/Code Info: Expiration Date of 11-26-24.

Quantity Affected: 914 lbs. total

Reason for Recall

Cheese curds may be contaminated with generic E. coli.

Distribution

WI

Type: Voluntary: Firm initiated

Recall Initiated: 2024-09-29

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

Westby Cooperative Creamery has 2 FDA actions in our database, including 2 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 (Westby Cooperative Creamery) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Westby Cooperative Creamery have FDA actions?

Westby Cooperative Creamery has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0125-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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