RecallHawk
Class III Recall

Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case

Hoff & Pepper, Co LLC.

Summary

The FDA issued a Class III for Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case by Hoff & Pepper, Co LLC.. Reason: Undeclared Allergen - Wheat.

Details

Source

Food Recall

External ID

F-1544-2024

Action Date

2024-08-07

Status

Terminated

Category

food

Product Description

Corey B's Oh Baby BBQ Sauce packaged in 12.6oz glass flask - 12 bottles per case

Lot/Code Info: Batch Numbers: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and 13 Best By Dates: 2/16/25, 2/17/25, 3/8/25, 4/14/25, 5/4/25, 6/19/25, 6/29/25, 7/11/25, 9/26/25, 10/25/25, 1/23/26, 3/7/26 and 4/18/26

Quantity Affected: 4,248 bottles

Reason for Recall

Undeclared Allergen - Wheat

Distribution

Alabama, Alaska, Arizona, Arkansas, California, Colorado Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Idaho, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming *Foreign locations: Quebec, Nova Scotia, Guam, District of Columbia, Alberta, Australia, Newfoundland

Type: Voluntary: Firm initiated

Recall Initiated: 2024-07-11

Company

Hoff & Pepper, Co LLC.

Chattanooga, TN

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 105 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Hoff & Pepper, Co LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Hoff & Pepper, Co LLC. have FDA actions?

This is the only FDA action we have on record for Hoff & Pepper, Co LLC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1544-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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