Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
Summary
The FDA issued a Class II for Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432 by ZB Importing LLC. Reason: Elevated levels of lead.
Details
Source
Food Recall
External ID
F-0830-2023
Action Date
2023-05-17
Status
Terminated
Category
food
Product Description
Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
Lot/Code Info: LOT 21321G2 Best by 01/2024
Quantity Affected: 3,456 units
Reason for Recall
Elevated levels of lead
Distribution
AL, AR, AZ, CA, CT, DE, FL, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NM, NV, NY, OH, OK, PA, PR, SC, TN, TX, USVI, UT, VA, VT, WA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-25
Company
Cicero, IL
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 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.
ZB Importing LLC has 8 FDA actions in our database, including 8 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 (ZB Importing LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ZB Importing LLC have FDA actions?
ZB Importing LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0830-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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