RecallHawk
Class I Recall

SWEET & SMOKY BBQ Packaged in 50lb kraft paper bags

Mane Inc

Summary

The FDA issued a Class I for SWEET & SMOKY BBQ Packaged in 50lb kraft paper bags by Mane Inc. Reason: Ingredient used in manufacturing tested positive for Salmonella.

Details

Source

Food Recall

External ID

F-0875-2021

Action Date

2021-08-25

Status

Terminated

Category

food

Product Description

SWEET & SMOKY BBQ Packaged in 50lb kraft paper bags

Lot/Code Info: Batch Numbers: 0000695758 Product Number: E_1933055 Best Buy Dates: 01/06/2022

Quantity Affected: 3,000lbs

Reason for Recall

Ingredient used in manufacturing tested positive for Salmonella

Distribution

Distributed to Manufacturers located in: Ohio, Indiana, Minnesota, and Oregon

Type: Voluntary: Firm initiated

Recall Initiated: 2021-08-09

Company

Mane Inc

Lebanon, OH

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Mane Inc has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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

How often does Mane Inc have FDA actions?

Mane Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0875-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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