Class IITerminatedVoluntary: Firm initiated
Singh Trading Inc. DBA Roshni Foods: food recall H-0172-2026
Singh Trading Inc. DBA Roshni Foods of Laurel, MD recalled Roshni Cinnamon Powder, 3.5 oz (100g). This product is packaged in clear plastic pouches. Reason: Product may contain elevated levels of lead and chromium. The FDA listed it as Class II in its Enforcement Report dated Nov 19, 2025; distribution: Florida, Maryland, North Carolina, Pennsylvania, Virginia.
Record status as published: Terminated (terminated Apr 29, 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
- Roshni Cinnamon Powder, 3.5 oz (100g). This product is packaged in clear plastic pouches.
- Product quantity
- 48 cases
- Reason for recall
- Product may contain elevated levels of lead and chromium.
- Codes, lots and dates on the package
- Batch No. 2409191
- Distribution pattern
- The adulterated product was distributed to the following states: VA,NC, PA,MD,FL
- Recalling firm
- Singh Trading Inc. DBA Roshni Foods, Laurel, MD
- 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
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 9, 2025 |
| Classified by the FDA | Nov 7, 2025 |
| Published in the Enforcement Report | Nov 19, 2025 |
| Terminated | Apr 29, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0172-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.