Shahzada brand Pulses and Spices; Cinnamon Powder; 7 oz (200g); packaged in clear plastic zip-top bags
Summary
The FDA issued a Class II for Shahzada brand Pulses and Spices; Cinnamon Powder; 7 oz (200g); packaged in clea by Advance Food International Inc.. Reason: Product contains elevated levels of lead (2,030 ppb).
Details
Source
Food Recall
External ID
F-1742-2024
Action Date
2024-08-28
Status
Terminated
Category
food
Product Description
Shahzada brand Pulses and Spices; Cinnamon Powder; 7 oz (200g); packaged in clear plastic zip-top bags
Lot/Code Info: No codes.
Quantity Affected: 120 packets
Reason for Recall
Product contains elevated levels of lead (2,030 ppb)
Distribution
NY, MA, NJ, CT
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-21
Company
Maspeth, 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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Advance Food International 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 (Advance Food International Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Advance Food International Inc. have FDA actions?
Advance Food International 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-1742-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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