Caribbean Belize LLC recalls Caribbean Rub spices due to undeclared wheat allergen. Consumers should check lot numbers and contact the company for details.
“Caribbean Belize Spices Caribbean Rub Recall: Undeclared Wheat Allergen Hazard.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/14372-caribbean-belize-spices-caribbean-rub-recall-undeclared-wheat-allergen-hazard. Based on FDA recall #F-0775-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0775-2021%22&limit=1).
Caribbean Belize LLC voluntarily recalled Caribbean Belize Spices Caribbean Rub due to undeclared wheat allergens, the FDA announced on July 2, 2021. The recall covers 9 bottles distributed in California, Michigan, South Carolina, New York, Iowa, and Illinois.
How to tell if you have it
Brand: Caribbean Belize
Product: Caribbean Belize Spices Caribbean Rub
Size: Net Wt. 3.5oz (99g) Plastic bottle with black cap
Lot Number: 0304232106
Best By Date: 04/23/24
Units Affected: 9 bottles
The hazard
The product contains undeclared wheat allergens, posing a risk to individuals with wheat allergies. The FDA classified the recall as Class II.
Context
GovInfoNow's records show other recent recalls of similar products include MID EAST Jordanian Zaatar Spice Mix Recall (2026-03-06), Bharat Bazar SOMA Kitchen Asafoetida Recall (2025-12-05), and Carousel Candies Choceur Holiday Bark Recall (2025-11-21).
How to tell if you have this one
Check for the lot number 0304232106 on the plastic bottle with a black cap. The product was sold as single bottles with a net weight of 3.5oz (99g) and best by date 04/23/24.
Brand
Caribbean Belize
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the lot number 0304232106 on the plastic bottle with a black cap.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “CA, MI, SC, NY, IA, IL.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Illinois, Iowa, Michigan, New York, South Carolina.
Recall timeline
FDA terminated this recall 3 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-0775-2021 (July 2, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0775-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.