The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case
Summary
The FDA issued a Class III for The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per by The Mustard Man Inc. Reason: Wrong Product in packaging - Simply Peppered Mustard bottles were filled with Simply Horsey Mustard.
Details
Source
Food Recall
External ID
F-0283-2022
Action Date
2021-12-22
Status
Terminated
Category
food
Product Description
The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case
Lot/Code Info: Batch Number - BB101322 Product Numbers: SH0001-6, SP0001-6 Manufacturing Numbers: FGMM2635, FGMM2633 Best By: 10/13/22
Quantity Affected: 1739 bottles
Reason for Recall
Wrong Product in packaging - Simply Peppered Mustard bottles were filled with Simply Horsey Mustard
Distribution
Florida, Illinois, Indiana, Michigan, North Carolina, Ohio, Pennsylvania, West Virginia
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-12
Company
Massillon, OH
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 42 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 (The Mustard Man Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Mustard Man Inc have FDA actions?
This is the only FDA action we have on record for The Mustard Man Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0283-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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