RecallHawk
Class II Recall

US Foods: Peanut Butter Toffee Bar, 3.4oz unit size, packaged in flow wrap, 24 packages per case

Killer Brownie Ltd

Summary

The FDA issued a Class II for US Foods: Peanut Butter Toffee Bar, 3.4oz unit size, packaged in flow wrap, 24 p by Killer Brownie Ltd. Reason: Foreign Material - Plastic.

Details

Source

Food Recall

External ID

F-1512-2023

Action Date

2023-09-20

Status

Terminated

Category

food

Product Description

US Foods: Peanut Butter Toffee Bar, 3.4oz unit size, packaged in flow wrap, 24 packages per case

Lot/Code Info: Lot No. 203KB650PR3, 203KB650MX3 Product No. 1020435

Quantity Affected: 82,080 units

Reason for Recall

Foreign Material - Plastic

Distribution

Distributed to IL

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-31

Company

Killer Brownie Ltd

Miamisburg, 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 28 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 (Killer Brownie Ltd) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Killer Brownie Ltd have FDA actions?

This is the only FDA action we have on record for Killer Brownie Ltd in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1512-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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