“Jelly Belly Licorice Bridge Mix: Gluten Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16880-jelly-belly-licorice-bridge-mix-gluten-contamination-risk. Based on FDA recall #F-1594-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1594-2019%22&limit=1).
The Food and Drug Administration announced on July 16, 2019, that Jelly Belly is voluntarily recalling Jelly Belly Licorice Bridge Mix because the product is labeled gluten-free but contains wheat flour. The agency classified this as a Class II recall.
How to tell if you have it
Jelly Belly Licorice Bridge Mix
Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy
UPC: 071567981675
Lot Code: 190321
Best Before Sep 21, 2020
The hazard
The confectionary bag states the product is Gluten Free, while the ingredient statement lists wheat flour. This mislabeling poses a risk to consumers with gluten sensitivities or celiac disease.
Context
GovInfoNow's records show other recent recalls of similar products include Uncle Giuseppe's Milk Chocolate Bridge Mix (2026-04-20) and Koi Koi Trading Fish Balls Recall (2026-01-28). Ghirardelli Frappe Mix Recall occurred on 2026-04-26.
How to tell if you have this one
Check for the UPC code 071567981675 on the product packaging. The product was manufactured with lot code 190321 and has a best before date of September 21, 2020.
Brand
Jelly Belly
Product
Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Packaging
Look for the UPC code 071567981675 on the packaging to identify affected items.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 25 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Nationwide, AL,FL,GA,IA,IL,IN, KS, KY, MA, MD, MI, MN, MO, NC, ND,NY, OH, OK, PA, SC, SD,TN, TX, VA, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 49 days 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-1594-2019 (July 16, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1594-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.