Galil Importing Corp is recalling Lior brand Cinnamon Ground Seasoning because the product contains elevated levels of lead. The recall affects 162 cases distributed across New York, New Jersey, Pennsylvania, Texas, Florida, and Illinois. No specific remedy or return instructions are currently listed in the record. Read more at govinfonow.com/recall/1434246-galil-importing-corp-recalls-lior-brand-cinnamon-ground-seasoning-90g.
“Lior Cinnamon Ground Seasoning Recalled for Lead Contamination.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/1434246-galil-importing-corp-recalls-lior-brand-cinnamon-ground-seasoning-90g. Based on FDA recall #H-1402-2026.
The FDA announced on Sept. 24, 2026, that Galil Importing Corp voluntarily recalled Lior brand Cinnamon Ground Seasoning due to elevated lead levels. Owners should discard the product.
How to tell if you have it
Brand: Lior
Product: Cinnamon Ground Seasoning
Packaging: 90g transparent plastic container
UPC: 794711005484
Code: GAP11304 printed on the side of the container under the ingredient line
The hazard
The product contains elevated levels of lead, according to the FDA.
Context
GovInfoNow's records show other recent recalls of similar products include BaiLiFeng Dried Cinnamon Recalled for High Lead Levels (2025-10-24), Venzu Traders Cinnamon Powder Recall: Lead Contamination Risk (2025-11-14), and DEVI Cinnamon Powder Recall: Lead Contamination Risk (2025-10-16).
How to tell if you have this one
Look for Lior brand Cinnamon Ground Seasoning in a 90g transparent plastic container. Check for UPC 794711005484 and GAP11304 printed on the side of the container under the ingredient line.
Brand
Lior
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop consuming the product
Do not eat the recalled Lior Cinnamon Ground Seasoning due to elevated lead levels.
Check your container
Verify if you have the 90g transparent plastic container with UPC 794711005484 and GAP11304 printed on the side.
Monitor for updates
Since no remedy is stated in the record, check official sources for future instructions on returns or refunds.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “NY, NJ, PA, TX, FL, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Illinois, New Jersey, New York, Pennsylvania, Texas.
Recall timeline
FDA published this recall 13 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
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 #H-1402-2026 (September 24, 2026)
Plain-language summary written by qwen3.6:35b-a3b on October 13, 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.