Roshni Cinnamon Powder, 3.5 oz (100g). This product is packaged in clear plastic pouches.
Summary
The FDA issued a Class II for Roshni Cinnamon Powder, 3.5 oz (100g). This product is packaged in clear plastic by Singh Trading Inc. DBA Roshni Foods. Reason: Product may contain elevated levels of lead and chromium..
Details
Source
Food Recall
External ID
H-0172-2026
Action Date
2025-11-19
Status
Terminated
Category
food
Product Description
Roshni Cinnamon Powder, 3.5 oz (100g). This product is packaged in clear plastic pouches.
Lot/Code Info: Batch No. 2409191
Quantity Affected: 48 cases
Reason for Recall
Product may contain elevated levels of lead and chromium.
Distribution
The adulterated product was distributed to the following states: VA,NC, PA,MD,FL
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-09
Company
Laurel, MD
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 44 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 (Singh Trading Inc. DBA Roshni Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Singh Trading Inc. DBA Roshni Foods have FDA actions?
This is the only FDA action we have on record for Singh Trading Inc. DBA Roshni Foods in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0172-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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