Class IITerminatedVoluntary: Firm initiated
Homeneeds Inc: food recall H-0208-2026
Homeneeds Inc of Bellevue, WA recalled DEVI brand Cinnamon Powder (Dalchini Powder), net wt.: 3.5 oz (100 g), packaged in flexible plastic bag. UPC 6 09595… Reason: Elevated levels of lead. FDA ground cinnamon sample was found to contain 2.92 mg/kg. The FDA listed it as Class II in its Enforcement Report dated Dec 3, 2025; distribution: Washington.
Record status as published: Terminated (terminated Jan 9, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 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.
- Codes, lots and dates on the package
- Batch # 2502315
- Distribution pattern
- distributed in WA.
- Recalling firm
- Homeneeds Inc, Bellevue, WA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Other
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 16, 2025 |
| Classified by the FDA | Nov 24, 2025 |
| Published in the Enforcement Report | Dec 3, 2025 |
| Terminated | Jan 9, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0208-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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