BBQ Seasoning Packaged in 50lb poly bag/cardboard box combo and kraft paper bags
Summary
The FDA issued a Class I for BBQ Seasoning Packaged in 50lb poly bag/cardboard box combo and kraft paper bags by Mane Inc. Reason: Ingredient used in manufacturing tested positive for Salmonella.
Details
Source
Food Recall
External ID
F-0874-2021
Action Date
2021-08-25
Status
Terminated
Category
food
Product Description
BBQ Seasoning Packaged in 50lb poly bag/cardboard box combo and kraft paper bags
Lot/Code Info: Batch Numbers: 0000700205, 0000700206, 0000682167 Product Number: S-1265-3, E20100846 Best Buy Dates: 01/15/2022, 12/09/2021
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
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-0874-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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