DEVI brand Cinnamon Powder (Dalchini Powder), net wt.: 3.5 oz (100 g), packaged in flexible plastic bag. UPC 6 09595 119
Summary
The FDA issued a Class II for DEVI brand Cinnamon Powder (Dalchini Powder), net wt.: 3.5 oz (100 g), packaged by Homeneeds Inc. Reason: Elevated levels of lead. FDA ground cinnamon sample was found to contain 2.92 mg/kg..
Details
Source
Food Recall
External ID
H-0208-2026
Action Date
2025-12-03
Status
Terminated
Category
food
Product Description
DEVI brand Cinnamon Powder (Dalchini Powder), net wt.: 3.5 oz (100 g), packaged in flexible plastic bag. UPC 6 09595 11904 5. Imported and Distributed by Homeneeds Inc. Bellevue, WA 98007; Product of India
Lot/Code Info: Batch # 2502315
Quantity Affected: 7 cases (total 140/100g packets)
Reason for Recall
Elevated levels of lead. FDA ground cinnamon sample was found to contain 2.92 mg/kg.
Distribution
distributed in WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-16
Company
Bellevue, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 18 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Homeneeds Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Homeneeds Inc have FDA actions?
This is the only FDA action we have on record for Homeneeds Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0208-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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