RecallHawk
Class II Recall

Member's Mark - Mild Cheddar Fancy (Fine) Shredded Cheese packaged in 5lbs, 8 packages per case

Biery Cheese Company

Summary

The FDA issued a Class II for Member's Mark - Mild Cheddar Fancy (Fine) Shredded Cheese packaged in 5lbs, 8 pa by Biery Cheese Company. Reason: Foreign Material - Glove remnants.

Details

Source

Food Recall

External ID

F-0720-2024

Action Date

2024-01-24

Status

Terminated

Category

food

Product Description

Member's Mark - Mild Cheddar Fancy (Fine) Shredded Cheese packaged in 5lbs, 8 packages per case

Lot/Code Info: Run # 36699681 Lot # 0506242331218 Product # 15401 Catalog # 980225088 Manufacturer # 39-211 Best By 06 May 2024

Quantity Affected: 320 cases

Reason for Recall

Foreign Material - Glove remnants

Distribution

Illinois, Indiana, Missouri, and Ohio

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-18

Company

Biery Cheese Company

Louisville, OH

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 81 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 (Biery Cheese Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Biery Cheese Company have FDA actions?

This is the only FDA action we have on record for Biery Cheese Company in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0720-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions