Lower riskFood recall · FDA · Published August 23, 2021
Jimbo's Bloody Mary Mix Recall: Unlabeled Soy, Sulfites, Wheat in Product
Jimbo's Kitchen recalls Bloody Mary Mix due to unlabeled soy, sulfites, and wheat in the product. Consumers should check for the UPC 787562000999 and contact the company for details.
“Jimbo's Bloody Mary Mix Recall: Unlabeled Soy, Sulfites, Wheat in Product.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14180-jimbo-s-bloody-mary-mix-recall-unlabeled-soy-sulfites-wheat. Based on FDA recall #F-0982-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0982-2021%22&limit=1).
The FDA announced on Aug. 23, 2021, that Jimbo's Kitchen voluntarily recalled its Bloody Mary Mix because the product contains undeclared soy, sulfites, and wheat. Consumers who purchased the item should stop using it immediately.
How to tell if you have it
Brand: Jimbo's Kitchen
Product: Jimbo's BLOODY MARY MIX; 2.5OZ MAKES ABOUT 45 SERVINGS
UPC: 7 87562 00099 9
Distribution: ME, NH, VT, MA
The hazard
The product contains soy, sulfites, and wheat that are not declared in the ingredient statement. The mix is hand-made in a facility that also processes wheat, dairy, eggs, and nuts.
Context
GovInfoNow's records show other recent recalls of similar products include Troemner Farm Pfeffernusse Cookies (2025-12-19), Nuts.com Espresso Malted Milk Balls (2026-03-10), and Sendero Gorditas de Azucar (2026-03-06).
How to tell if you have this one
Check for the UPC code 787562000999 on the product label. The product is sold in 2.5oz containers that make about 45 servings.
Brand
Jimbo's Kitchen
Product
Jimbo's BLOODY MARY MIX; 2.5OZ MAKES ABOUT 45 SERVINGS; Ingredients: Horseradish Powder, Parsley, Worcestershire
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC code 787562000999 on the product label to confirm it's part of the recall.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “ME, NH, VT, MA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maine, Massachusetts, New Hampshire, Vermont.
Recall timeline
FDA terminated this recall 18 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
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-0982-2021 (August 23, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0982-2021 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.