Stop using nowFood recall · FDA · Published March 4, 2024
La Fiesta Cinnamon Ground Recall: Lead Contamination Risk
La Fiesta's cinnamon ground product contains elevated lead levels. Consumers should stop using this item due to potential health risks from lead exposure.
“La Fiesta Cinnamon Ground Recall: Lead Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/9553-la-fiesta-cinnamon-ground-recall-lead-contamination-risk. Based on FDA recall #F-1093-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1093-2024%22&limit=1).
La Fiesta Food Products voluntarily recalled La Fiesta Canela Molida, Cinnamon Ground, 0.87oz (24.8g) due to elevated levels of lead, the FDA said on March 4, 2024.
How to tell if you have it
La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), UPC #032327000449
Lot code 25033
The hazard
The product contains elevated levels of lead.
Context
GovInfoNow's records show La Fiesta Food Products has two other recalls on record since February 2, 2022. On January 22, 2025, the company issued a recall for bread crumbs due to an undeclared sesame allergen hazard. Other recent recalls of similar products include Haitai Cinnamon Powder Recall (October 17, 2025), Venzu Traders Cinnamon Powder Recall (November 14, 2025), and DEVI Cinnamon Powder Recall (October 16, 2025).
How to tell if you have this one
Look for La Fiesta Canela Molida (Cinnamon Ground) in 0.87oz (24.8g) cello bags with UPC #032327000449. The lot code is 25033.
Brand
La Fiesta
Product
La Fiesta, Canela Molida, Cinnamon Ground, 0.87oz (24.8g), UPC #032327000449, packed in cello bags
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Immediately stop using the recalled cinnamon ground product as it contains elevated lead levels that pose a health risk.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “U.S. distribution to 319 retailers in California, Arizona, Washington and Texas.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Texas, Washington.
Recall timeline
FDA terminated this recall 6 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-1093-2024 (March 4, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1093-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.