Lower riskFood recall · FDA · Published October 12, 2021
The Mustard Man Inc Simply Peppered Mustard Recall: Wrong Product in Packaging
The Mustard Man Inc recalls 8oz Simply Peppered Mustard bottles that were filled with Simply Horsey Mustard. Consumers should check batch numbers and return affected products.
“The Mustard Man Inc Simply Peppered Mustard Recall: Wrong Product in Packaging.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14027-the-mustard-man-inc-simply-peppered-mustard-recall-wrong-product. Based on FDA recall #F-0283-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0283-2022%22&limit=1).
The Food and Drug Administration announced on Oct. 12, 2021, that The Mustard Man Inc voluntarily recalled Simply Peppered Mustard 8oz plastic bottles due to mislabeling. The hazard involves Simply Horsey Mustard being incorrectly filled into the Simply Peppered Mustard containers.
How to tell if you have it
Brand: The Mustard Man Inc
Product: Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case
Batch Number: BB101322
Product Numbers: SH0001-6, SP0001-6
Manufacturing Numbers: FGMM2635, FGMM2633
Best By: 10/13/22
The hazard
The recall involves Simply Peppered Mustard bottles that were filled with Simply Horsey Mustard. This constitutes a wrong product in packaging error.
Context
GovInfoNow's records show Savannah Bee Company issued a honey BBQ sauce mustard recall on Feb. 27, 2026, for undeclared soy and wheat allergens. Ventura Foods recalled Carolina-Style Mustard BBQ Sauce on Nov. 6, 2025, due to foreign objects in the sauce. New Way Import recalled preserved mustard on Nov. 19, 2025, for undeclared wheat.
How to tell if you have this one
Check for batch number BB101322 on the bottle. The product is 8oz plastic bottles, 6 per case, with product numbers SH0001-6 or SP0001-6.
Brand
The Mustard Man Inc
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for batch number BB101322 on the bottle label.
Where it went and when
Where it was distributed
Distributed in 8 states.
Listed by the agency
Not listed
FDA distribution: “Florida, Illinois, Indiana, Michigan, North Carolina, Ohio, Pennsylvania, West Virginia” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Illinois, Indiana, Michigan, North Carolina, Ohio, Pennsylvania, West Virginia.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0283-2022 (October 12, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0283-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.