ALB Flavor brand CINNAMON Powder; 100 g; ALB-USA Enterprises Inc 529 Bryant Av, Bronx, NY 10474; UPC 5 304000 333362; pa
Summary
The FDA issued a Class II for ALB Flavor brand CINNAMON Powder; 100 g; ALB-USA Enterprises Inc 529 Bryant Av, by Alb-USA Enterprises Inc. Reason: Product contains elevated levels of lead (3.294ppm).
Details
Source
Food Recall
External ID
F-1757-2024
Action Date
2024-09-04
Status
Terminated
Category
food
Product Description
ALB Flavor brand CINNAMON Powder; 100 g; ALB-USA Enterprises Inc 529 Bryant Av, Bronx, NY 10474; UPC 5 304000 333362; packaged in a plastic bag inside a brown carton box with an image of cinnamon powder and two cinnamon sticks centered at the bottom.
Lot/Code Info: Best Before date of 30/08/2025 Lot number LA02.
Quantity Affected: 240 units
Reason for Recall
Product contains elevated levels of lead (3.294ppm)
Distribution
NY, CT, MI, MA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-25
Company
Bronx, NY
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 (Alb-USA Enterprises Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Alb-USA Enterprises Inc have FDA actions?
This is the only FDA action we have on record for Alb-USA Enterprises Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1757-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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