El Servidor Corp Ground Cinnamon Net Wt. 1.5 oz. UPC: 745245113244. Packaged in clear plastic bag. 12 bags per case. Gut
Summary
The FDA issued a Class II for El Servidor Corp Ground Cinnamon Net Wt. 1.5 oz. UPC: 745245113244. Packaged in by Gutierrez Distributors, LLC. Reason: Elevated lead levels in cinnamon.
Details
Source
Food Recall
External ID
F-1754-2024
Action Date
2024-09-04
Status
Ongoing
Category
food
Product Description
El Servidor Corp Ground Cinnamon Net Wt. 1.5 oz. UPC: 745245113244. Packaged in clear plastic bag. 12 bags per case. Gutierrez Distributor Canela Molida Ground Cinnamon 1.5 oz. UPC: 852705000164 Packaged in clear plastic bag.
Quantity Affected: 5 cases
Reason for Recall
Elevated lead levels in cinnamon
Distribution
Distributed to wholesaler in NY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-08-16
Company
Passaic, 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.
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 (Gutierrez Distributors, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gutierrez Distributors, LLC have FDA actions?
This is the only FDA action we have on record for Gutierrez Distributors, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1754-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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