Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25 oz clear plastics jars with black lids. UPC
Summary
The FDA issued a Class II for Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25 oz c by Colonna Brothers Inc.. Reason: Elevated lead levels in cinnamon.
Details
Source
Food Recall
External ID
F-1753-2024
Action Date
2024-09-04
Status
Terminated
Category
food
Product Description
Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25 oz clear plastics jars with black lids. UPC: 639277656377 Marcum brand ground cinnamon packaged in 1.5 oz clear plastic jars with black lids. UPC:051933364035
Lot/Code Info: Best By: 10/06/25 10A11 Best By 12/05/25 12 D8 Best By 12/05/25 12 D11
Quantity Affected: unknown
Reason for Recall
Elevated lead levels in cinnamon
Distribution
Distributed to retail stores nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-30
Company
North Bergen, NJ
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 24 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Colonna Brothers Inc. has 2 FDA actions in our database, including 2 recalls.
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 (Colonna Brothers Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Colonna Brothers Inc. have FDA actions?
Colonna Brothers Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1753-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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